Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98391920T>A , CM000669.2:g.98391920T>A | GRCh38 |
| NC_000007.13:g.98021232T>A , CM000669.1:g.98021232T>A | GRCh37 |
| NC_000007.12:g.97859168T>A | NCBI36 |
| NG_013090.1:g.14196A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005260.9:c.51+8882A>T MANE Select | ENSP00000005260.8:n.51+8882A>T | |
| ENST00000005260.8:c.51+8882A>T | ENSP00000005260.8:n.51+8882A>T | |
| ENST00000462558.5:n.267+8882A>T | ||
| ENST00000479789.1:n.357+8061A>T | ||
| NM_018842.4:c.51+8882A>T | NP_061330.2:n.51+8882A>T | |
| NM_018842.5:c.51+8882A>T MANE Select | NP_061330.2:n.51+8882A>T |