Linked Data
dbSNP Id:
rs751033365
ExAC:
5:56178063 C / G
gnomAD v2:
5-56178063-C-G
gnomAD v3:
5-56882236-C-G
gnomAD v4:
5-56882236-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.56882236C>G , CM000667.2:g.56882236C>G | GRCh38 |
| NC_000005.9:g.56178063C>G , CM000667.1:g.56178063C>G | GRCh37 |
| NC_000005.8:g.56213820C>G | NCBI36 |
| NG_031884.1:g.72164C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399503.4:c.3036C>G MANE Select | ENSP00000382423.3:p.Cys1012Trp | |
| ENST00000399503.3:c.3036C>G | ENSP00000382423.3:p.Cys1012Trp | |
| NM_005921.1:c.3036C>G | NP_005912.1:p.Cys1012Trp | |
| XM_005248519.3:c.2658C>G | XP_005248576.2:p.Cys886Trp | |
| XM_011543406.1:c.2781C>G | XP_011541708.1:p.Cys927Trp | |
| XM_011543407.1:c.2757C>G | XP_011541709.1:p.Cys919Trp | |
| XM_011543408.1:c.3036C>G | XP_011541710.1:p.Cys1012Trp | |
| XM_017009484.1:c.2625C>G | XP_016864973.1:p.Cys875Trp | |
| XM_017009485.1:c.2547C>G | XP_016864974.1:p.Cys849Trp | |
| XR_001742068.2:n.3067C>G | ||
| NM_005921.2:c.3036C>G MANE Select | NP_005912.1:p.Cys1012Trp |