Linked Data
ClinVar Variation Id:
196935
dbSNP Id:
rs201251963
ExAC:
11:76910768 A / G
gnomAD v2:
11-76910768-A-G
gnomAD v3:
11-77199723-A-G
gnomAD v4:
11-77199723-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.77199723A>G , CM000673.2:g.77199723A>G | GRCh38 |
| NC_000011.9:g.76910768A>G , CM000673.1:g.76910768A>G | GRCh37 |
| NC_000011.8:g.76588416A>G | NCBI36 |
| NG_009086.1:g.76459A>G | |
| NG_009086.2:g.76478A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409709.9:c.4757A>G MANE Select | ENSP00000386331.3:p.Asn1586Ser | |
| ENST00000670577.1:c.2598A>G | ||
| ENST00000409619.6:c.4610A>G | ENSP00000386635.2:p.Asn1537Ser | |
| ENST00000409709.7:c.4757A>G | ENSP00000386331.3:p.Asn1586Ser | |
| ENST00000458169.2:c.2186A>G | ENSP00000417017.2:p.Asn729Ser | |
| ENST00000458637.6:c.4643A>G | ENSP00000392185.2:p.Asn1548Ser | |
| ENST00000481328.7:n.2296A>G | ||
| NM_000260.3:c.4757A>G | NP_000251.3:p.Asn1586Ser | |
| NM_001127180.1:c.4643A>G | NP_001120652.1:p.Asn1548Ser | |
| XM_005274012.2:c.4643A>G | XP_005274069.1:p.Asn1548Ser | |
| XM_006718558.2:c.4751A>G | XP_006718621.1:p.Asn1584Ser | |
| XM_006718559.2:c.4643A>G | XP_006718622.1:p.Asn1548Ser | |
| XM_006718560.2:c.4643A>G | XP_006718623.1:p.Asn1548Ser | |
| XM_006718561.2:c.4643A>G | XP_006718624.1:p.Asn1548Ser | |
| XM_011545044.1:c.4757A>G | XP_011543346.1:p.Asn1586Ser | |
| XM_011545045.1:c.4751A>G | XP_011543347.1:p.Asn1584Ser | |
| XM_011545046.1:c.4724A>G | XP_011543348.1:p.Asn1575Ser | |
| XM_011545047.1:c.4661A>G | XP_011543349.1:p.Asn1554Ser | |
| XM_011545048.1:c.4532A>G | XP_011543350.1:p.Asn1511Ser | |
| XM_011545049.1:c.4520A>G | XP_011543351.1:p.Asn1507Ser | |
| XM_011545050.1:c.4493A>G | XP_011543352.1:p.Asn1498Ser | |
| XM_011545051.1:c.4757A>G | XP_011543353.1:p.Asn1586Ser | |
| XM_011545052.1:c.4757A>G | XP_011543354.1:p.Asn1586Ser | |
| XR_949938.1:n.5077A>G | ||
| XR_949941.1:n.5077A>G | ||
| XR_949942.1:n.5079A>G | ||
| XM_011545044.2:c.4757A>G | XP_011543346.1:p.Asn1586Ser | |
| XM_011545046.2:c.4847A>G | XP_011543348.2:p.Asn1616Ser | |
| XM_011545050.2:c.4493A>G | XP_011543352.1:p.Asn1498Ser | |
| XM_017017778.1:c.4841A>G | XP_016873267.1:p.Asn1614Ser | |
| XM_017017779.1:c.4841A>G | XP_016873268.1:p.Asn1614Ser | |
| XM_017017780.1:c.4847A>G | XP_016873269.1:p.Asn1616Ser | |
| XM_017017781.1:c.4751A>G | XP_016873270.1:p.Asn1584Ser | |
| XM_017017782.1:c.4733A>G | XP_016873271.1:p.Asn1578Ser | |
| XM_017017783.1:c.4733A>G | XP_016873272.1:p.Asn1578Ser | |
| XM_017017784.1:c.4733A>G | XP_016873273.1:p.Asn1578Ser | |
| XM_017017785.1:c.4610A>G | XP_016873274.1:p.Asn1537Ser | |
| XM_017017786.1:c.4847A>G | XP_016873275.1:p.Asn1616Ser | |
| XM_017017788.1:c.4733A>G | XP_016873277.1:p.Asn1578Ser | |
| XR_001747885.1:n.4862A>G | ||
| XR_001747886.1:n.4862A>G | ||
| XR_001747887.1:n.4862A>G | ||
| XR_001747888.1:n.4862A>G | ||
| NM_000260.4:c.4757A>G MANE Select | NP_000251.3:p.Asn1586Ser | |
| NM_001127180.2:c.4643A>G | NP_001120652.1:p.Asn1548Ser | |
| NM_001369365.1:c.4610A>G | NP_001356294.1:p.Asn1537Ser |