Linked Data
dbSNP Id:
rs774481269
ExAC:
3:93615465 G / T
gnomAD v2:
3-93615465-G-T
gnomAD v3:
3-93896621-G-T
gnomAD v4:
3-93896621-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.93896621G>T , CM000665.2:g.93896621G>T | GRCh38 |
| NC_000003.11:g.93615465G>T , CM000665.1:g.93615465G>T | GRCh37 |
| NC_000003.10:g.95098155G>T | NCBI36 |
| NG_009813.1:g.82470C>A , LRG_572:g.82470C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348974.5:c.920C>A | ENSP00000330021.7:p.Ala307Glu | |
| ENST00000394236.9:c.920C>A MANE Select | ENSP00000377783.3:p.Ala307Glu | |
| ENST00000407433.6:c.875C>A | ENSP00000385794.2:p.Ala292Glu | |
| ENST00000647936.1:c.920C>A | ENSP00000496822.1:p.Ala307Glu | |
| ENST00000648381.1:n.1088C>A | ||
| ENST00000648853.1:c.878C>A | ENSP00000497262.1:p.Ala293Glu | |
| ENST00000649103.1:c.1019C>A | ENSP00000497962.1:n.1019C>A | |
| ENST00000650591.1:c.1016C>A | ENSP00000497376.1:p.Ala339Glu | |
| ENST00000394236.7:c.920C>A | ENSP00000377783.3:p.Ala307Glu | |
| ENST00000407433.5:c.527C>A | ENSP00000385794.1:p.Ala176Glu | |
| NM_000313.3:c.920C>A , LRG_572t1:c.920C>A | NP_000304.2:p.Ala307Glu | |
| NM_001314077.1:c.1016C>A , LRG_572t2:c.1016C>A | NP_001301006.1:p.Ala339Glu | |
| NM_000313.4:c.920C>A MANE Select | NP_000304.2:p.Ala307Glu | |
| NM_001314077.2:c.1016C>A | NP_001301006.1:p.Ala339Glu |