Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117830248A>T , CM000670.2:g.117830248A>T | GRCh38 |
| NC_000008.10:g.118842487A>T , CM000670.1:g.118842487A>T | GRCh37 |
| NC_000008.9:g.118911668A>T | NCBI36 |
| NG_007455.2:g.286572T>A , LRG_493:g.286572T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.1266T>A MANE Select | NP_000118.2:p.Ile422= |
| ENST00000378204.7:c.1266T>A MANE Select | ENSP00000367446.3:p.Ile422= |
| NM_000127.2:c.1266T>A , LRG_493t1:c.1266T>A | NP_000118.2:p.Ile422= |
| ENST00000378204.6:c.1266T>A | ENSP00000367446.2:p.Ile422= |
| ENST00000436216.1:c.689T>A | |
| ENST00000436216.2:c.689T>A | |
| ENST00000437196.1:c.*157T>A | ENSP00000407299.1:n.*157T>A |
| ENST00000684189.1:n.733T>A |