Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96301675A>G , CM000664.2:g.96301675A>G | GRCh38 |
| NC_000002.11:g.96967413A>G , CM000664.1:g.96967413A>G | GRCh37 |
| NC_000002.10:g.96331140A>G | NCBI36 |
| NG_016973.1:g.8885T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.423T>C MANE Select | NP_054733.2:p.Ala141= |
| ENST00000323853.10:c.423T>C MANE Select | ENSP00000317123.5:p.Ala141= |
| NM_014014.4:c.423T>C | NP_054733.2:p.Ala141= |
| ENST00000323853.9:c.423T>C | ENSP00000317123.5:p.Ala141= |
| ENST00000652267.1:c.423T>C | ENSP00000498933.1:p.Ala141= |