Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814696G>C , CM000664.2:g.218814696G>C | GRCh38 |
| NC_000002.11:g.219679419G>C , CM000664.1:g.219679419G>C | GRCh37 |
| NC_000002.10:g.219387663G>C | NCBI36 |
| NG_007959.1:g.37948G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.1415G>C MANE Select | NP_000775.1:p.Gly472Ala |
| ENST00000258415.9:c.1415G>C MANE Select | ENSP00000258415.4:p.Gly472Ala |
| NM_000784.3:c.1415G>C | NP_000775.1:p.Gly472Ala |
| ENST00000258415.8:c.1415G>C | ENSP00000258415.4:p.Gly472Ala |
| ENST00000494263.5:n.2127G>C | |
| XM_017003488.2:c.995G>C | XP_016858977.1:p.Gly332Ala |