Linked Data
ClinVar Variation Id:
281235
dbSNP Id:
rs748704263
ExAC:
2:71892421 C / A
gnomAD v2:
2-71892421-C-A
gnomAD v3:
2-71665291-C-A
gnomAD v4:
2-71665291-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71665291C>A , CM000664.2:g.71665291C>A | GRCh38 |
| NC_000002.11:g.71892421C>A , CM000664.1:g.71892421C>A | GRCh37 |
| NC_000002.10:g.71745929C>A | NCBI36 |
| NG_008694.1:g.216669C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2718C>A | ENSP00000513536.1:p.Ser906= | |
| ENST00000698058.1:c.1935C>A | ENSP00000513537.1:p.Ser645= | |
| ENST00000698059.1:c.2043C>A | ENSP00000513538.1:p.Ser681= | |
| ENST00000258104.8:c.5187C>A MANE Plus Clinical | ENSP00000258104.3:p.Ser1729= | |
| ENST00000410020.8:c.5304C>A MANE Select | ENSP00000386881.3:p.Ser1768= | |
| ENST00000258104.7:c.5187C>A | ENSP00000258104.3:p.Ser1729= | |
| ENST00000394120.6:c.5190C>A | ENSP00000377678.2:p.Ser1730= | |
| ENST00000409366.5:c.5253C>A | ENSP00000386512.1:p.Ser1751= | |
| ENST00000409582.7:c.5301C>A | ENSP00000386547.3:p.Ser1767= | |
| ENST00000409651.5:c.5283C>A | ENSP00000386683.1:p.Ser1761= | |
| ENST00000409744.5:c.5211C>A | ENSP00000386285.1:p.Ser1737= | |
| ENST00000409762.5:c.5238C>A | ENSP00000387137.1:p.Ser1746= | |
| ENST00000410020.7:c.5304C>A | ENSP00000386881.3:p.Ser1768= | |
| ENST00000410041.1:c.5241C>A | ENSP00000386617.1:p.Ser1747= | |
| ENST00000413539.6:c.5280C>A | ENSP00000407046.2:p.Ser1760= | |
| ENST00000429174.6:c.5250C>A | ENSP00000398305.2:p.Ser1750= | |
| ENST00000479049.6:n.2072C>A | ||
| NM_001130455.1:c.5190C>A | NP_001123927.1:p.Ser1730= | |
| NM_001130976.1:c.5145C>A | NP_001124448.1:p.Ser1715= | |
| NM_001130977.1:c.5208C>A | NP_001124449.1:p.Ser1736= | |
| NM_001130978.1:c.5250C>A | NP_001124450.1:p.Ser1750= | |
| NM_001130979.1:c.5280C>A | NP_001124451.1:p.Ser1760= | |
| NM_001130980.1:c.5238C>A | NP_001124452.1:p.Ser1746= | |
| NM_001130981.1:c.5301C>A | NP_001124453.1:p.Ser1767= | |
| NM_001130982.1:c.5283C>A | NP_001124454.1:p.Ser1761= | |
| NM_001130983.1:c.5253C>A | NP_001124455.1:p.Ser1751= | |
| NM_001130984.1:c.5211C>A | NP_001124456.1:p.Ser1737= | |
| NM_001130985.1:c.5241C>A | NP_001124457.1:p.Ser1747= | |
| NM_001130986.1:c.5148C>A | NP_001124458.1:p.Ser1716= | |
| NM_001130987.1:c.5304C>A | NP_001124459.1:p.Ser1768= | |
| NM_003494.3:c.5187C>A | NP_003485.1:p.Ser1729= | |
| XM_005264584.3:c.5346C>A | XP_005264641.1:p.Ser1782= | |
| XM_005264585.3:c.5343C>A | XP_005264642.1:p.Ser1781= | |
| XM_005264584.4:c.5346C>A | XP_005264641.1:p.Ser1782= | |
| XM_005264585.5:c.5343C>A | XP_005264642.1:p.Ser1781= | |
| NM_001130987.2:c.5304C>A MANE Select | NP_001124459.1:p.Ser1768= | |
| NM_001130455.2:c.5190C>A | NP_001123927.1:p.Ser1730= | |
| NM_001130976.2:c.5145C>A | NP_001124448.1:p.Ser1715= | |
| NM_001130977.2:c.5208C>A | NP_001124449.1:p.Ser1736= | |
| NM_001130978.2:c.5250C>A | NP_001124450.1:p.Ser1750= | |
| NM_001130979.2:c.5280C>A | NP_001124451.1:p.Ser1760= | |
| NM_001130980.2:c.5238C>A | NP_001124452.1:p.Ser1746= | |
| NM_001130981.2:c.5301C>A | NP_001124453.1:p.Ser1767= | |
| NM_001130982.2:c.5283C>A | NP_001124454.1:p.Ser1761= | |
| NM_001130983.2:c.5253C>A | NP_001124455.1:p.Ser1751= | |
| NM_001130984.2:c.5211C>A | NP_001124456.1:p.Ser1737= | |
| NM_001130985.2:c.5241C>A | NP_001124457.1:p.Ser1747= | |
| NM_001130986.2:c.5148C>A | NP_001124458.1:p.Ser1716= | |
| NM_003494.4:c.5187C>A MANE Plus Clinical | NP_003485.1:p.Ser1729= |