Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98391905A>T , CM000669.2:g.98391905A>T | GRCh38 |
| NC_000007.13:g.98021217A>T , CM000669.1:g.98021217A>T | GRCh37 |
| NC_000007.12:g.97859153A>T | NCBI36 |
| NG_013090.1:g.14211T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005260.9:c.51+8897T>A MANE Select | ENSP00000005260.8:n.51+8897T>A | |
| ENST00000005260.8:c.51+8897T>A | ENSP00000005260.8:n.51+8897T>A | |
| ENST00000462558.5:n.267+8897T>A | ||
| ENST00000479789.1:n.357+8076T>A | ||
| NM_018842.4:c.51+8897T>A | NP_061330.2:n.51+8897T>A | |
| NM_018842.5:c.51+8897T>A MANE Select | NP_061330.2:n.51+8897T>A |