Linked Data
ClinVar Variation Id:
212062
ClinVar RCV Id:
RCV000194076
RCV000861106
RCV001117064
RCV001117062
RCV001117063
RCV001833139
RCV001698998
RCV002517128
dbSNP Id:
rs146197239
ExAC:
16:53675264 A / C
gnomAD v2:
16-53675264-A-C
gnomAD v3:
16-53641352-A-C
gnomAD v4:
16-53641352-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53641352A>C , CM000678.2:g.53641352A>C | GRCh38 |
| NC_000016.9:g.53675264A>C , CM000678.1:g.53675264A>C | GRCh37 |
| NC_000016.8:g.52232765A>C | NCBI36 |
| NG_008991.2:g.67508T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262135.9:c.2807T>G | ENSP00000262135.4:p.Ile936Ser | |
| ENST00000565343.2:n.3231T>G | ||
| ENST00000621565.5:c.2807T>G | ENSP00000480698.1:p.Ile936Ser | |
| ENST00000647211.2:c.2807T>G MANE Select | ENSP00000493946.1:p.Ile936Ser | |
| ENST00000680193.1:c.2807T>G | ENSP00000506379.1:p.Ile936Ser | |
| ENST00000681587.1:n.819T>G | ||
| ENST00000262135.8:c.2807T>G | ENSP00000262135.4:p.Ile936Ser | |
| ENST00000379925.7:c.2807T>G | ENSP00000369257.3:p.Ile936Ser | |
| ENST00000563746.5:c.2807T>G | ENSP00000457889.1:p.Ile936Ser | |
| ENST00000564374.5:c.2807T>G | ENSP00000456534.1:p.Ile936Ser | |
| ENST00000621565.4:c.2807T>G | ENSP00000480698.1:p.Ile936Ser | |
| NM_001127897.1:c.2807T>G | NP_001121369.1:p.Ile936Ser | |
| NM_001127897.2:c.2807T>G | NP_001121369.1:p.Ile936Ser | |
| NM_001308334.1:c.2807T>G | NP_001295263.1:p.Ile936Ser | |
| NM_015272.2:c.2807T>G | NP_056087.2:p.Ile936Ser | |
| NM_015272.3:c.2807T>G | NP_056087.2:p.Ile936Ser | |
| XM_005255867.1:c.2807T>G | XP_005255924.1:p.Ile936Ser | |
| XM_005255868.1:c.2819T>G | XP_005255925.1:p.Ile940Ser | |
| XM_005255871.2:c.1052T>G | XP_005255928.1:p.Ile351Ser | |
| XM_011522968.1:c.2807T>G | XP_011521270.1:p.Ile936Ser | |
| XM_011522969.1:c.2819T>G | XP_011521271.1:p.Ile940Ser | |
| XM_011522970.1:c.2819T>G | XP_011521272.1:p.Ile940Ser | |
| XM_011522971.1:c.2819T>G | XP_011521273.1:p.Ile940Ser | |
| XM_011522972.1:c.2819T>G | XP_011521274.1:p.Ile940Ser | |
| XM_011522973.1:c.2819T>G | XP_011521275.1:p.Ile940Ser | |
| XM_011522974.1:c.1052T>G | XP_011521276.1:p.Ile351Ser | |
| XR_933260.1:n.2851T>G | ||
| NM_001127897.3:c.2807T>G | NP_001121369.1:p.Ile936Ser | |
| NM_001308334.2:c.2807T>G | NP_001295263.1:p.Ile936Ser | |
| NM_001330538.1:c.2807T>G | NP_001317467.1:p.Ile936Ser | |
| NM_015272.4:c.2807T>G | NP_056087.2:p.Ile936Ser | |
| XM_005255868.2:c.2819T>G | XP_005255925.1:p.Ile940Ser | |
| XM_011522970.2:c.2819T>G | XP_011521272.1:p.Ile940Ser | |
| XM_011522971.3:c.2819T>G | XP_011521273.1:p.Ile940Ser | |
| XM_011522973.3:c.2819T>G | XP_011521275.1:p.Ile940Ser | |
| XM_017023094.2:c.2819T>G | XP_016878583.1:p.Ile940Ser | |
| XM_017023095.2:c.2819T>G | XP_016878584.1:p.Ile940Ser | |
| XM_017023096.2:c.2819T>G | XP_016878585.1:p.Ile940Ser | |
| XM_017023098.1:c.1052T>G | XP_016878587.1:p.Ile351Ser | |
| XM_017023099.1:c.1052T>G | XP_016878588.1:p.Ile351Ser | |
| XR_933260.3:n.2862T>G | ||
| NM_015272.5:c.2807T>G MANE Select | NP_056087.2:p.Ile936Ser | |
| NM_001127897.4:c.2807T>G | NP_001121369.1:p.Ile936Ser | |
| NM_001330538.2:c.2807T>G | NP_001317467.1:p.Ile936Ser | |
| NM_001308334.3:c.2807T>G | NP_001295263.1:p.Ile936Ser |