Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110176885C>G , CM000675.2:g.110176885C>G | GRCh38 |
| NC_000013.10:g.110829232C>G , CM000675.1:g.110829232C>G | GRCh37 |
| NC_000013.9:g.109627233C>G | NCBI36 |
| NG_011544.2:g.135265G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.2869G>C MANE Select | NP_001836.3:p.Gly957Arg |
| ENST00000375820.10:c.2869G>C MANE Select | ENSP00000364979.4:p.Gly957Arg |
| NM_001845.5:c.2869G>C | NP_001836.3:p.Gly957Arg |
| ENST00000375820.8:c.2869G>C | ENSP00000364979.4:p.Gly957Arg |
| XM_011521048.1:c.2677G>C | XP_011519350.1:p.Gly893Arg |
| XM_011521048.2:c.2677G>C | XP_011519350.1:p.Gly893Arg |