Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128286770C>A , CM000667.2:g.128286770C>A | GRCh38 |
| NC_000005.9:g.127622462C>A , CM000667.1:g.127622462C>A | GRCh37 |
| NC_000005.8:g.127650361C>A | NCBI36 |
| NG_008750.1:g.256274G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001999.4:c.6960G>T MANE Select | NP_001990.2:p.Met2320Ile |
| ENST00000262464.9:c.6960G>T MANE Select | ENSP00000262464.4:p.Met2320Ile |
| NM_001999.3:c.6960G>T | NP_001990.2:p.Met2320Ile |
| ENST00000262464.8:c.6960G>T | ENSP00000262464.4:p.Met2320Ile |
| ENST00000508053.5:c.6960G>T | ENSP00000424571.1:p.Met2320Ile |
| ENST00000619499.4:c.6957G>T | ENSP00000482132.1:p.Met2319Ile |
| ENST00000703783.1:n.3744G>T | |
| XM_017009228.2:c.6807G>T | XP_016864717.1:p.Met2269Ile |