Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155812032C>G , CM000669.2:g.155812032C>G | GRCh38 |
| NC_000007.13:g.155604726C>G , CM000669.1:g.155604726C>G | GRCh37 |
| NC_000007.12:g.155297487C>G | NCBI36 |
| NG_007504.2:g.5242G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000193.4:c.91G>C MANE Select | NP_000184.1:p.Gly31Arg |
| ENST00000297261.7:c.91G>C MANE Select | ENSP00000297261.2:p.Gly31Arg |
| NM_000193.2:c.91G>C | NP_000184.1:p.Gly31Arg |
| NM_000193.3:c.91G>C | NP_000184.1:p.Gly31Arg |
| ENST00000297261.6:c.91G>C | ENSP00000297261.2:p.Gly31Arg |