Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128369290C>T , CM000667.2:g.128369290C>T | GRCh38 |
| NC_000005.9:g.127704983C>T , CM000667.1:g.127704983C>T | GRCh37 |
| NC_000005.8:g.127732882C>T | NCBI36 |
| NG_008750.1:g.173753G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2140G>A MANE Select | ENSP00000262464.4:p.Val714Met | |
| ENST00000262464.8:c.2140G>A | ENSP00000262464.4:p.Val714Met | |
| ENST00000508053.5:c.2140G>A | ENSP00000424571.1:p.Val714Met | |
| ENST00000508989.5:c.2041G>A | ENSP00000425596.1:p.Val681Met | |
| ENST00000511489.1:n.361G>A | ||
| ENST00000619499.4:c.2137G>A | ENSP00000482132.1:p.Val713Met | |
| NM_001999.3:c.2140G>A | NP_001990.2:p.Val714Met | |
| XM_017009228.2:c.1987G>A | XP_016864717.1:p.Val663Met | |
| NM_001999.4:c.2140G>A MANE Select | NP_001990.2:p.Val714Met |