Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29232313C>G , CM000664.2:g.29232313C>G | GRCh38 |
| NC_000002.11:g.29455179C>G , CM000664.1:g.29455179C>G | GRCh37 |
| NC_000002.10:g.29308683C>G | NCBI36 |
| NG_009445.1:g.694254G>C , LRG_488:g.694254G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.2623G>C MANE Select | NP_004295.2:p.Gly875Arg |
| ENST00000389048.8:c.2623G>C MANE Select | ENSP00000373700.3:p.Gly875Arg |
| NM_004304.4:c.2623G>C | NP_004295.2:p.Gly875Arg |
| ENST00000389048.7:c.2623G>C | ENSP00000373700.3:p.Gly875Arg |
| ENST00000618119.4:c.1492G>C | ENSP00000482733.1:p.Gly498Arg |
| XM_024452778.1:c.-151G>C | XP_024308546.1:n.-151G>C |
| XR_001738688.2:n.3553G>C |