Linked Data
dbSNP Id:
rs1172300265
gnomAD v2:
19-45296867-A-T
gnomAD v3:
19-44793610-A-T
gnomAD v4:
19-44793610-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44793610A>T , CM000681.2:g.44793610A>T | GRCh38 |
| NC_000019.9:g.45296867A>T , CM000681.1:g.45296867A>T | GRCh37 |
| NC_000019.8:g.49988707A>T | NCBI36 |
| NG_054718.1:g.20756A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647358.2:c.1274A>T MANE Select | ENSP00000494162.1:p.Glu425Val | |
| ENST00000270279.7:c.1274A>T | ENSP00000270279.3:p.Glu425Val | |
| ENST00000341505.4:c.1136A>T | ENSP00000340250.4:p.Glu379Val | |
| NM_001130852.1:c.1136A>T | NP_001124324.1:p.Glu379Val | |
| NM_012116.3:c.1274A>T | NP_036248.3:p.Glu425Val | |
| XM_005258696.2:c.1274A>T | XP_005258753.1:p.Glu425Val | |
| XM_011526688.1:c.1274A>T | XP_011524990.1:p.Glu425Val | |
| XM_011526689.1:c.1136A>T | XP_011524991.1:p.Glu379Val | |
| XR_935783.1:n.1221A>T | ||
| NM_012116.4:c.1274A>T MANE Select | NP_036248.3:p.Glu425Val | |
| XM_005258696.3:c.1274A>T | XP_005258753.1:p.Glu425Val | |
| XM_011526688.2:c.1274A>T | XP_011524990.1:p.Glu425Val | |
| XM_011526689.2:c.1136A>T | XP_011524991.1:p.Glu379Val | |
| XR_935783.2:n.1226A>T |