HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812341C>T , CM000669.2:g.155812341C>T | GRCh38 |
NC_000007.13:g.155605035C>T , CM000669.1:g.155605035C>T | GRCh37 |
NC_000007.12:g.155297796C>T | NCBI36 |
NG_007504.2:g.4933G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-219G>A MANE Select | ENSP00000297261.2:n.-219G>A | |
NM_000193.4:c.-219G>A MANE Select | NP_000184.1:n.-219G>A |