Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155461299T>A , CM000669.2:g.155461299T>A | GRCh38 |
| NC_000007.13:g.155253994T>A , CM000669.1:g.155253994T>A | GRCh37 |
| NC_000007.12:g.154946755T>A | NCBI36 |
| NG_007124.1:g.9580T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297375.4:c.686-1072T>A MANE Select | ENSP00000297375.4:n.686-1072T>A | |
| NM_001427.3:c.686-1072T>A | NP_001418.2:n.686-1072T>A | |
| NM_001427.4:c.686-1072T>A MANE Select | NP_001418.2:n.686-1072T>A |