Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766206G>T , CM000674.2:g.57766206G>T | GRCh38 |
| NC_000012.11:g.58159989G>T , CM000674.1:g.58159989G>T | GRCh37 |
| NC_000012.10:g.56446256G>T | NCBI36 |
| NG_007076.1:g.5988C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.108-9C>A | ||
| ENST00000713544.1:c.196-9C>A | ENSP00000518840.1:n.196-9C>A | |
| ENST00000713545.1:c.196-9C>A | ENSP00000518841.1:n.196-9C>A | |
| ENST00000228606.9:c.196-9C>A MANE Select | ENSP00000228606.4:n.196-9C>A | |
| ENST00000228606.8:c.196-9C>A | ENSP00000228606.4:n.196-9C>A | |
| ENST00000546496.1:n.24-9C>A | ||
| ENST00000546609.1:c.108-9C>A | ||
| ENST00000547344.5:n.250-9C>A | ||
| ENST00000552186.1:n.306C>A | ||
| NM_000785.3:c.196-9C>A | NP_000776.1:n.196-9C>A | |
| NM_000785.4:c.196-9C>A MANE Select | NP_000776.1:n.196-9C>A |