Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94001082G>T , CM000663.2:g.94001082G>T | GRCh38 |
| NC_000001.10:g.94466638G>T , CM000663.1:g.94466638G>T | GRCh37 |
| NC_000001.9:g.94239226G>T | NCBI36 |
| NG_009073.1:g.125068C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.6306C>A MANE Select | NP_000341.2:p.Asp2102Glu |
| ENST00000370225.4:c.6306C>A MANE Select | ENSP00000359245.3:p.Asp2102Glu |
| NM_000350.2:c.6306C>A | NP_000341.2:p.Asp2102Glu |
| ENST00000370225.3:c.6306C>A | ENSP00000359245.3:p.Asp2102Glu |
| ENST00000536513.5:c.2682C>A | ENSP00000439707.2:p.Asp894Glu |