Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571443C= , CM000663.2:g.154571443C= | GRCh38 |
| NC_000001.10:g.154543919C= , CM000663.1:g.154543919C= | GRCh37 |
| NC_000001.9:g.152810543C= | NCBI36 |
| NG_008027.1:g.8663C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.620C= MANE Select | ENSP00000357461.3:p.Ala207= | |
| ENST00000636034.1:c.620C= | ENSP00000489703.1:p.Ala207= | |
| ENST00000637900.1:c.626C= | ENSP00000490474.1:p.Ala209= | |
| ENST00000368476.3:c.620C= | ENSP00000357461.3:p.Ala207= | |
| NM_000748.2:c.620C= | NP_000739.1:p.Ala207= | |
| XM_017000180.2:c.110C= | XP_016855669.1:p.Ala37= | |
| XR_001736952.2:n.872C= | ||
| NM_000748.3:c.620C= MANE Select | NP_000739.1:p.Ala207= |