Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812617G>A , CM000664.2:g.218812617G>A | GRCh38 |
| NC_000002.11:g.219677340G>A , CM000664.1:g.219677340G>A | GRCh37 |
| NC_000002.10:g.219385584G>A | NCBI36 |
| NG_007959.1:g.35869G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000784.4:c.712G>A MANE Select | NP_000775.1:p.Val238Met |
| ENST00000258415.9:c.712G>A MANE Select | ENSP00000258415.4:p.Val238Met |
| NM_000784.3:c.712G>A | NP_000775.1:p.Val238Met |
| ENST00000258415.8:c.712G>A | ENSP00000258415.4:p.Val238Met |
| ENST00000411688.1:c.430G>A | ENSP00000392671.1:p.Val144Met |
| ENST00000445971.1:c.*173G>A | ENSP00000404945.1:n.*173G>A |
| ENST00000466602.1:n.660G>A | |
| ENST00000494263.5:n.1146G>A | |
| XM_017003488.2:c.292G>A | XP_016858977.1:p.Val98Met |