Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73641003G= , CM000664.2:g.73641003G= | GRCh38 |
| NC_000002.11:g.73868130G= , CM000664.1:g.73868130G= | GRCh37 |
| NC_000002.10:g.73721638G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272425.4:c.626C= MANE Select | ENSP00000272425.3:p.Ala209= | |
| ENST00000272425.3:c.626C= | ENSP00000272425.3:p.Ala209= | |
| NM_003960.3:c.626C= | NP_003951.3:p.Ala209= | |
| NM_003960.4:c.626C= MANE Select | NP_003951.3:p.Ala209= |