Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190408322G>C , CM000665.2:g.190408322G>C | GRCh38 |
| NC_000003.11:g.190126111G>C , CM000665.1:g.190126111G>C | GRCh37 |
| NC_000003.10:g.191608805G>C | NCBI36 |
| NG_008149.1:g.25271G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264734.3:c.391G>C MANE Select | ENSP00000264734.3:p.Gly131Arg | |
| ENST00000456423.2:c.115-1581G>C | ENSP00000414136.2:n.115-1581G>C | |
| ENST00000264734.2:c.601G>C | ENSP00000264734.2:p.Gly201Arg | |
| ENST00000456423.1:c.325-1581G>C | ENSP00000414136.1:n.325-1581G>C | |
| NM_006580.3:c.601G>C | NP_006571.1:p.Gly201Arg | |
| NM_001378492.1:c.391G>C | NP_001365421.1:p.Gly131Arg | |
| NM_001378493.1:c.391G>C | NP_001365422.1:p.Gly131Arg | |
| NM_006580.4:c.391G>C MANE Select | NP_006571.2:p.Gly131Arg |