Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150297807C>T , CM000667.2:g.150297807C>T | GRCh38 |
| NC_000005.9:g.149677370C>T , CM000667.1:g.149677370C>T | GRCh37 |
| NC_000005.8:g.149657563C>T | NCBI36 |
| NG_051250.1:g.10156G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001012301.4:c.1117G>A MANE Select | NP_001012301.1:p.Val373Met |
| ENST00000328668.8:c.1117G>A MANE Select | ENSP00000333395.7:p.Val373Met |
| NM_001012301.2:c.1117G>A | NP_001012301.1:p.Val373Met |
| NM_001012301.3:c.1117G>A | NP_001012301.1:p.Val373Met |
| ENST00000328668.7:c.1117G>A | ENSP00000333395.7:p.Val373Met |
| ENST00000515301.2:c.688G>A | ENSP00000426879.2:p.Val230Met |