HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536261A>T , CM000679.2:g.42536261A>T | GRCh38 |
NC_000017.10:g.40688279A>T , CM000679.1:g.40688279A>T | GRCh37 |
NC_000017.9:g.37941805A>T | NCBI36 |
NG_011552.1:g.5329A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.-12A>T MANE Select | ENSP00000225927.1:n.-12A>T | |
ENST00000225927.6:c.-12A>T | ENSP00000225927.1:n.-12A>T | |
NM_000263.3:c.-12A>T | NP_000254.2:n.-12A>T | |
XM_024450771.1:c.-12A>T | XP_024306539.1:n.-12A>T | |
NM_000263.4:c.-12A>T MANE Select | NP_000254.2:n.-12A>T |