Linked Data
dbSNP Id:
rs149978009
ExAC:
3:50357183 C / A
gnomAD v2:
3-50357183-C-A
gnomAD v4:
3-50319752-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.50319752C>A , CM000665.2:g.50319752C>A | GRCh38 |
| NC_000003.11:g.50357183C>A , CM000665.1:g.50357183C>A | GRCh37 |
| NC_000003.10:g.50332187C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357750.9:c.738G>T MANE Select | ENSP00000350387.4:p.Thr246= | |
| ENST00000357750.8:c.738G>T | ENSP00000350387.4:p.Thr246= | |
| ENST00000395139.7:c.738G>T | ENSP00000378571.3:p.Thr246= | |
| ENST00000442581.1:c.738G>T | ENSP00000406657.1:p.Thr246= | |
| ENST00000447092.5:c.738G>T | ENSP00000401853.1:p.Thr246= | |
| ENST00000481597.5:n.873G>T | ||
| NM_003773.4:c.738G>T | NP_003764.3:p.Thr246= | |
| NM_033158.4:c.738G>T | NP_149348.2:p.Thr246= | |
| XM_005265524.1:c.738G>T | XP_005265581.1:p.Thr246= | |
| XM_005265525.1:c.738G>T | XP_005265582.1:p.Thr246= | |
| XM_005265524.2:c.738G>T | XP_005265581.1:p.Thr246= | |
| XM_005265525.2:c.738G>T | XP_005265582.1:p.Thr246= | |
| NM_003773.5:c.738G>T MANE Select | NP_003764.3:p.Thr246= | |
| NM_033158.5:c.738G>T | NP_149348.2:p.Thr246= |