HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586866G>A , CM000679.2:g.41586866G>A | GRCh38 |
NC_000017.10:g.39743118G>A , CM000679.1:g.39743118G>A | GRCh37 |
NC_000017.9:g.36996644G>A | NCBI36 |
NG_008624.1:g.5030C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.-32C>T MANE Select | ENSP00000167586.6:n.-32C>T | |
ENST00000167586.6:c.-32C>T | ENSP00000167586.6:n.-32C>T | |
NM_000526.4:c.-32C>T | NP_000517.2:n.-32C>T | |
NM_000526.5:c.-32C>T MANE Select | NP_000517.3:n.-32C>T |