Linked Data
ClinVar Variation Id:
739453
ClinVar RCV Id:
RCV000915422
dbSNP Id:
rs771208077
ExAC:
4:107016747 G / A
gnomAD v2:
4-107016747-G-A
gnomAD v4:
4-106095590-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.106095590G>A , CM000666.2:g.106095590G>A | GRCh38 |
| NC_000004.11:g.107016747G>A , CM000666.1:g.107016747G>A | GRCh37 |
| NC_000004.10:g.107236196G>A | NCBI36 |
| NG_034057.2:g.230906C>T | |
| NG_034057.3:g.226094C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000273980.10:c.2463C>T | ENSP00000273980.4:p.Ala821= | |
| ENST00000394708.7:c.2463C>T MANE Select | ENSP00000378198.2:p.Ala821= | |
| ENST00000273980.9:c.2463C>T | ENSP00000273980.4:p.Ala821= | |
| ENST00000361687.8:c.2274C>T | ENSP00000355338.4:p.Ala758= | |
| ENST00000394706.7:c.2346C>T | ENSP00000378196.3:p.Ala782= | |
| ENST00000394708.6:c.2463C>T | ENSP00000378198.2:p.Ala821= | |
| ENST00000432496.6:c.2463C>T | ENSP00000405847.2:p.Ala821= | |
| ENST00000467183.6:c.*2102C>T | ENSP00000421182.1:n.*2102C>T | |
| ENST00000510927.5:n.2116C>T | ||
| NM_001163435.2:c.2463C>T | NP_001156907.1:p.Ala821= | |
| NM_001163436.2:c.2463C>T | NP_001156908.1:p.Ala821= | |
| NM_001163437.2:c.2346C>T | NP_001156909.1:p.Ala782= | |
| NM_001290768.1:c.1947C>T | NP_001277697.1:p.Ala649= | |
| NM_033115.4:c.2274C>T | NP_149106.2:p.Ala758= | |
| XM_011532417.1:c.2463C>T | XP_011530719.1:p.Ala821= | |
| XM_011532418.1:c.2145C>T | XP_011530720.1:p.Ala715= | |
| XM_011532419.1:c.1947C>T | XP_011530721.1:p.Ala649= | |
| XM_011532417.2:c.2463C>T | XP_011530719.1:p.Ala821= | |
| XM_017008846.1:c.2463C>T | XP_016864335.1:p.Ala821= | |
| XM_017008847.2:c.2463C>T | XP_016864336.1:p.Ala821= | |
| XM_017008848.1:c.2145C>T | XP_016864337.1:p.Ala715= | |
| XM_017008849.1:c.1947C>T | XP_016864338.1:p.Ala649= | |
| XM_024454281.1:c.2463C>T | XP_024310049.1:p.Ala821= | |
| XM_024454282.1:c.2463C>T | XP_024310050.1:p.Ala821= | |
| XR_002959772.1:n.2657C>T | ||
| NM_001163435.3:c.2463C>T MANE Select | NP_001156907.2:p.Ala821= | |
| NM_001163436.4:c.2463C>T | NP_001156908.2:p.Ala821= | |
| NM_001163437.3:c.2346C>T | NP_001156909.2:p.Ala782= | |
| NM_001290768.2:c.1947C>T | NP_001277697.2:p.Ala649= | |
| NM_033115.5:c.2274C>T | NP_149106.3:p.Ala758= |