Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.144398264C>T , CM000669.2:g.144398264C>T | GRCh38 |
| NC_000007.13:g.144095357C>T , CM000669.1:g.144095357C>T | GRCh37 |
| NC_000007.12:g.143726290C>T | NCBI36 |
| NG_028979.1:g.16964G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080413.3:c.1774+18G>A MANE Select | NP_001073882.3:n.1774+18G>A |
| ENST00000467773.1:c.1774+18G>A MANE Select | ENSP00000419457.1:n.1774+18G>A |
| ENST00000483238.5:c.1678+18G>A | ENSP00000419565.1:n.1678+18G>A |
| ENST00000643164.1:c.871+18G>A | ENSP00000495343.1:n.871+18G>A |
| ENST00000645489.1:c.1423+18G>A | ENSP00000496732.1:n.1423+18G>A |
| XM_011515791.1:c.1423+18G>A | XP_011514093.1:n.1423+18G>A |
| XM_017011742.2:c.1678+18G>A | XP_016867231.1:n.1678+18G>A |