Linked Data
dbSNP Id:
rs754417128
ExAC:
16:28847535 A / T
gnomAD v2:
16-28847535-A-T
gnomAD v4:
16-28836214-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28836214A>T , CM000678.2:g.28836214A>T | GRCh38 |
| NC_000016.9:g.28847535A>T , CM000678.1:g.28847535A>T | GRCh37 |
| NC_000016.8:g.28755036A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336783.9:c.3177A>T MANE Select | ENSP00000338718.4:p.Arg1059Ser | |
| ENST00000325215.10:c.3139+38A>T | ENSP00000315650.6:n.3139+38A>T | |
| ENST00000336783.8:c.3177A>T | ENSP00000338718.4:p.Arg1059Ser | |
| ENST00000340394.12:c.3085+92A>T | ENSP00000341459.8:n.3085+92A>T | |
| ENST00000382686.8:c.3085+92A>T | ENSP00000372133.4:n.3085+92A>T | |
| ENST00000395547.6:c.3139+38A>T | ENSP00000378917.2:n.3139+38A>T | |
| ENST00000562583.5:c.1152A>T | ENSP00000456162.2:p.Arg384Ser | |
| ENST00000563314.5:n.3551A>T | ||
| ENST00000564162.1:c.280+92A>T | ENSP00000455427.1:n.280+92A>T | |
| ENST00000564304.5:c.3157+38A>T | ENSP00000457613.1:n.3157+38A>T | |
| ENST00000565971.5:c.2241A>T | ENSP00000457599.1:n.2241A>T | |
| ENST00000566007.5:c.354+92A>T | ||
| ENST00000566946.5:c.1155A>T | ENSP00000454757.1:p.Arg385Ser | |
| ENST00000570200.5:c.3139+38A>T | ENSP00000454516.1:n.3139+38A>T | |
| NM_001308230.1:c.3157+38A>T | NP_001295159.1:n.3157+38A>T | |
| NM_007245.3:c.3177A>T | NP_009176.2:p.Arg1059Ser | |
| NM_017492.3:c.3139+38A>T | NP_059867.3:n.3139+38A>T | |
| NM_145714.2:c.3139+38A>T | NP_663760.1:n.3139+38A>T | |
| NM_148414.2:c.3139+38A>T | NP_680780.1:n.3139+38A>T | |
| NM_148415.2:c.3085+92A>T | NP_680781.1:n.3085+92A>T | |
| NM_148416.2:c.3085+92A>T | NP_680782.1:n.3085+92A>T | |
| XM_005255061.1:c.3160+38A>T | XP_005255118.1:n.3160+38A>T | |
| XM_005255062.1:c.3160+38A>T | XP_005255119.1:n.3160+38A>T | |
| XM_005255063.2:c.3160+38A>T | XP_005255120.1:n.3160+38A>T | |
| XM_005255064.1:c.3157+38A>T | XP_005255121.1:n.3157+38A>T | |
| XM_005255065.1:c.3142+38A>T | XP_005255122.1:n.3142+38A>T | |
| XM_005255066.1:c.3139+38A>T | XP_005255123.1:n.3139+38A>T | |
| XM_005255067.1:c.3106+92A>T | XP_005255124.1:n.3106+92A>T | |
| XM_005255068.1:c.3106+92A>T | XP_005255125.1:n.3106+92A>T | |
| XM_005255069.1:c.3198A>T | XP_005255126.1:p.Arg1066Ser | |
| XM_005255070.1:c.3160+38A>T | XP_005255127.1:n.3160+38A>T | |
| XM_005255071.1:c.3160+38A>T | XP_005255128.1:n.3160+38A>T | |
| XM_005255074.1:c.3106+92A>T | XP_005255131.1:n.3106+92A>T | |
| XM_005255075.1:c.3106+92A>T | XP_005255132.1:n.3106+92A>T | |
| XM_005255076.1:c.3103+92A>T | XP_005255133.1:n.3103+92A>T | |
| XM_005255077.1:c.2980+38A>T | XP_005255134.1:n.2980+38A>T | |
| XM_006721007.1:c.3088+38A>T | XP_006721070.1:n.3088+38A>T | |
| XM_006721008.1:c.3070+38A>T | XP_006721071.1:n.3070+38A>T | |
| XM_006721009.1:c.3160+38A>T | XP_006721072.1:n.3160+38A>T | |
| XM_006721010.2:c.3160+38A>T | XP_006721073.1:n.3160+38A>T | |
| XM_006721011.1:c.3106+92A>T | XP_006721074.1:n.3106+92A>T | |
| XM_006721012.2:c.3106+92A>T | XP_006721075.1:n.3106+92A>T | |
| XM_006721013.2:c.3106+92A>T | XP_006721076.1:n.3106+92A>T | |
| XM_011545719.1:c.3160+38A>T | XP_011544021.1:n.3160+38A>T | |
| XM_011545720.1:c.3160+38A>T | XP_011544022.1:n.3160+38A>T | |
| XM_011545721.1:c.3106+92A>T | XP_011544023.1:n.3106+92A>T | |
| XM_011545722.1:c.2794+38A>T | XP_011544024.1:n.2794+38A>T | |
| XR_243256.1:n.3407A>T | ||
| XM_005255063.4:c.3160+38A>T | XP_005255120.1:n.3160+38A>T | |
| XM_006721012.4:c.3106+92A>T | XP_006721075.1:n.3106+92A>T | |
| XM_011545719.2:c.3160+38A>T | XP_011544021.1:n.3160+38A>T | |
| XM_017022891.1:c.2962+38A>T | XP_016878380.1:n.2962+38A>T | |
| XM_017022892.1:c.2776+38A>T | XP_016878381.1:n.2776+38A>T | |
| XR_001751820.1:n.3410A>T | ||
| NM_001308230.2:c.3157+38A>T | NP_001295159.1:n.3157+38A>T | |
| NM_001387166.1:c.3157+38A>T | NP_001374095.1:n.3157+38A>T | |
| NM_001387167.1:c.3139+38A>T | NP_001374096.1:n.3139+38A>T | |
| NM_001387168.1:c.3139+38A>T | NP_001374097.1:n.3139+38A>T | |
| NM_001387169.1:c.3103+92A>T | NP_001374098.1:n.3103+92A>T | |
| NM_001387170.1:c.3103+92A>T | NP_001374099.1:n.3103+92A>T | |
| NM_001387171.1:c.3198A>T | NP_001374100.1:p.Arg1066Ser | |
| NM_001387172.1:c.3195A>T | NP_001374101.1:p.Arg1065Ser | |
| NM_001387173.1:c.3088+92A>T | NP_001374102.1:n.3088+92A>T | |
| NM_001387174.1:c.3085+92A>T | NP_001374103.1:n.3085+92A>T | |
| NM_001387175.1:c.3085+92A>T | NP_001374104.1:n.3085+92A>T | |
| NM_001387176.1:c.3085+92A>T | NP_001374105.1:n.3085+92A>T | |
| NM_001387177.1:c.3085+92A>T | NP_001374106.1:n.3085+92A>T | |
| NM_001387178.1:c.3180A>T | NP_001374107.1:p.Arg1060Ser | |
| NM_001387179.1:c.3067+38A>T | NP_001374108.1:n.3067+38A>T | |
| NM_001387180.1:c.3171A>T | NP_001374109.1:p.Arg1057Ser | |
| NM_001387181.1:c.3160+38A>T | NP_001374110.1:n.3160+38A>T | |
| NM_001387182.1:c.3157+38A>T | NP_001374111.1:n.3157+38A>T | |
| NM_001387183.1:c.3142+38A>T | NP_001374112.1:n.3142+38A>T | |
| NM_001387184.1:c.3142+38A>T | NP_001374113.1:n.3142+38A>T | |
| NM_001387185.1:c.3013+92A>T | NP_001374114.1:n.3013+92A>T | |
| NM_001387186.1:c.3108A>T | NP_001374115.1:p.Arg1036Ser | |
| NM_001387187.1:c.3108A>T | NP_001374116.1:p.Arg1036Ser | |
| NM_001387188.1:c.3105A>T | NP_001374117.1:p.Arg1035Ser | |
| NM_001387189.1:c.3103+92A>T | NP_001374118.1:n.3103+92A>T | |
| NM_001387190.1:c.3103+92A>T | NP_001374119.1:n.3103+92A>T | |
| NM_001387191.1:c.3088+92A>T | NP_001374120.1:n.3088+92A>T | |
| NM_001387192.1:c.3088+92A>T | NP_001374121.1:n.3088+92A>T | |
| NM_001387193.1:c.3103+92A>T | NP_001374122.1:n.3103+92A>T | |
| NM_001387194.1:c.3088+92A>T | NP_001374123.1:n.3088+92A>T | |
| NM_001387195.1:c.3085+92A>T | NP_001374124.1:n.3085+92A>T | |
| NM_001387196.1:c.3085+92A>T | NP_001374125.1:n.3085+92A>T | |
| NM_001387197.1:c.3085+38A>T | NP_001374126.1:n.3085+38A>T | |
| NM_001387198.1:c.3085+92A>T | NP_001374127.1:n.3085+92A>T | |
| NM_001387199.1:c.3016+92A>T | NP_001374128.1:n.3016+92A>T | |
| NM_001387200.1:c.3031+92A>T | NP_001374129.1:n.3031+92A>T | |
| NM_001387202.1:c.3013+92A>T | NP_001374131.1:n.3013+92A>T | |
| NM_001387203.1:c.2988A>T | NP_001374132.1:p.Arg996Ser | |
| NM_001387204.1:c.2949+38A>T | NP_001374133.1:n.2949+38A>T | |
| NM_007245.4:c.3177A>T MANE Select | NP_009176.2:p.Arg1059Ser | |
| NM_017492.4:c.3139+38A>T | NP_059867.3:n.3139+38A>T | |
| NM_145714.3:c.3139+38A>T | NP_663760.1:n.3139+38A>T | |
| NM_148414.3:c.3139+38A>T | NP_680780.1:n.3139+38A>T | |
| NM_148415.3:c.3085+92A>T | NP_680781.1:n.3085+92A>T | |
| NM_148416.3:c.3085+92A>T | NP_680782.1:n.3085+92A>T |