Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94000861C>T , CM000663.2:g.94000861C>T | GRCh38 |
| NC_000001.10:g.94466417C>T , CM000663.1:g.94466417C>T | GRCh37 |
| NC_000001.9:g.94239005C>T | NCBI36 |
| NG_009073.1:g.125289G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.6454G>A MANE Select | NP_000341.2:p.Gly2152Ser |
| ENST00000370225.4:c.6454G>A MANE Select | ENSP00000359245.3:p.Gly2152Ser |
| NM_000350.2:c.6454G>A | NP_000341.2:p.Gly2152Ser |
| ENST00000370225.3:c.6454G>A | ENSP00000359245.3:p.Gly2152Ser |
| ENST00000536513.5:c.2830G>A | ENSP00000439707.2:p.Gly944Ser |