Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044172G>A , CM000672.2:g.114044172G>A | GRCh38 |
| NC_000010.10:g.115803931G>A , CM000672.1:g.115803931G>A | GRCh37 |
| NC_000010.9:g.115793921G>A | NCBI36 |
| NG_012187.1:g.5126G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.40G>A MANE Select | ENSP00000358301.2:p.Gly14Ser | |
| ENST00000369295.3:c.40G>A | ENSP00000358301.2:p.Gly14Ser | |
| NM_000684.2:c.40G>A | NP_000675.1:p.Gly14Ser | |
| NM_000684.3:c.40G>A MANE Select | NP_000675.1:p.Gly14Ser |