HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536241C= , CM000679.2:g.42536241C= | GRCh38 |
NC_000017.10:g.40688259C= , CM000679.1:g.40688259C= | GRCh37 |
NC_000017.9:g.37941785C= | NCBI36 |
NG_011552.1:g.5309C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.-32C= MANE Select | ENSP00000225927.1:n.-32C= | |
ENST00000225927.6:c.-32C= | ENSP00000225927.1:n.-32C= | |
NM_000263.3:c.-32C= | NP_000254.2:n.-32C= | |
XM_024450771.1:c.-32C= | XP_024306539.1:n.-32C= | |
NM_000263.4:c.-32C= MANE Select | NP_000254.2:n.-32C= |