Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65117630G>A , CM000673.2:g.65117630G>A | GRCh38 |
| NC_000011.9:g.64885102G>A , CM000673.1:g.64885102G>A | GRCh37 |
| NC_000011.8:g.64641678G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310597.6:c.24C>T MANE Select | ENSP00000308548.4:p.Gly8= | |
| ENST00000310597.5:c.24C>T | ENSP00000308548.4:p.Gly8= | |
| ENST00000528598.1:c.24C>T | ENSP00000436896.1:p.Gly8= | |
| NM_014205.3:c.24C>T | NP_055020.1:p.Gly8= | |
| NM_014205.4:c.24C>T MANE Select | NP_055020.1:p.Gly8= |