Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.61045821G>T , CM000664.2:g.61045821G>T | GRCh38 |
| NC_000002.11:g.61272956G>T , CM000664.1:g.61272956G>T | GRCh37 |
| NC_000002.10:g.61126460G>T | NCBI36 |
| NG_008665.1:g.33145G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002618.4:c.883G>T MANE Select | NP_002609.1:p.Ala295Ser |
| ENST00000295030.6:c.883G>T MANE Select | ENSP00000295030.4:p.Ala295Ser |
| NM_002618.3:c.883G>T | NP_002609.1:p.Ala295Ser |
| ENST00000295030.5:c.883G>T | ENSP00000295030.4:p.Ala295Ser |
| XM_011532904.1:c.766G>T | XP_011531206.1:p.Ala256Ser |