Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800163G>C , CM000666.2:g.24800163G>C | GRCh38 |
| NC_000004.11:g.24801785G>C , CM000666.1:g.24801785G>C | GRCh37 |
| NC_000004.10:g.24410883G>C | NCBI36 |
| NG_012213.1:g.9701G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.642G>C MANE Select | ENSP00000371554.3:p.Gly214= | |
| ENST00000382120.3:c.642G>C | ENSP00000371554.3:p.Gly214= | |
| NM_003102.2:c.642G>C | NP_003093.2:p.Gly214= | |
| XR_427488.1:n.832G>C | ||
| NM_003102.3:c.642G>C | NP_003093.2:p.Gly214= | |
| NM_003102.4:c.642G>C MANE Select | NP_003093.2:p.Gly214= |