Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20638104C= , CM000663.2:g.20638104C= | GRCh38 |
| NC_000001.10:g.20964597C= , CM000663.1:g.20964597C= | GRCh37 |
| NC_000001.9:g.20837184C= | NCBI36 |
| NG_008164.1:g.9650C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032409.3:c.650C= MANE Select | NP_115785.1:p.Ala217= |
| ENST00000321556.5:c.650C= MANE Select | ENSP00000364204.3:p.Ala217= |
| NM_032409.2:c.650C= | NP_115785.1:p.Ala217= |
| ENST00000321556.4:c.650C= | ENSP00000364204.3:p.Ala217= |