HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150992901G>A , CM000669.2:g.150992901G>A | GRCh38 |
NC_000007.13:g.150689989G>A , CM000669.1:g.150689989G>A | GRCh37 |
NC_000007.12:g.150320922G>A | NCBI36 |
NG_011992.1:g.6843G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297494.8:c.-51-852G>A MANE Select | ENSP00000297494.3:n.-51-852G>A | |
ENST00000297494.7:c.-51-852G>A | ENSP00000297494.3:n.-51-852G>A | |
ENST00000461406.5:c.-149+1601G>A | ENSP00000417143.1:n.-149+1601G>A | |
NM_000603.4:c.-51-852G>A | NP_000594.2:n.-51-852G>A | |
NM_000603.5:c.-51-852G>A MANE Select | NP_000594.2:n.-51-852G>A |