Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1433424C>T , CM000667.2:g.1433424C>T | GRCh38 |
| NC_000005.9:g.1433539C>T , CM000667.1:g.1433539C>T | GRCh37 |
| NC_000005.8:g.1486539C>T | NCBI36 |
| NG_015885.1:g.17005G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.419-726G>A MANE Select | ENSP00000270349.9:n.419-726G>A | |
| ENST00000270349.11:c.419-726G>A | ENSP00000270349.9:n.419-726G>A | |
| NM_001044.4:c.419-726G>A | NP_001035.1:n.419-726G>A | |
| NM_001044.5:c.419-726G>A MANE Select | NP_001035.1:n.419-726G>A |