Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26727914C>G , CM000664.2:g.26727914C>G | GRCh38 |
| NC_000002.11:g.26950782C>G , CM000664.1:g.26950782C>G | GRCh37 |
| NC_000002.10:g.26804286C>G | NCBI36 |
| NG_033884.1:g.40202C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302909.4:c.531C>G MANE Select | ENSP00000306275.3:p.Ala177= | |
| ENST00000302909.3:c.531C>G | ENSP00000306275.3:p.Ala177= | |
| ENST00000620977.1:c.162C>G | ENSP00000483136.1:p.Ala54= | |
| NM_002246.2:c.531C>G | NP_002237.1:p.Ala177= | |
| XM_005264293.1:c.201C>G | XP_005264350.1:p.Ala67= | |
| XM_005264293.2:c.201C>G | XP_005264350.1:p.Ala67= | |
| NM_002246.3:c.531C>G MANE Select | NP_002237.1:p.Ala177= |