HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218270451G>T , CM000664.2:g.218270451G>T | GRCh38 |
NC_000002.11:g.219135174G>T , CM000664.1:g.219135174G>T | GRCh37 |
NC_000002.10:g.218843418G>T | NCBI36 |
NG_017060.1:g.5060G>T | |
NG_033036.1:g.4720C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000691799.1:n.70+731G>T | ||
ENST00000248451.7:c.-85G>T | ENSP00000248451.3:n.-85G>T | |
NM_001077399.2:c.-85G>T | NP_001070867.1:n.-85G>T | |
NM_015488.4:c.-85G>T | NP_056303.3:n.-85G>T |