HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67437065C>A , CM000678.2:g.67437065C>A | GRCh38 |
NC_000016.9:g.67470968C>A , CM000678.1:g.67470968C>A | GRCh37 |
NC_000016.8:g.66028469C>A | NCBI36 |
NG_011482.1:g.49122G>T | |
NG_016549.1:g.10933C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.*62C>A MANE Select | ENSP00000316786.5:n.*62C>A | |
ENST00000326152.5:c.*62C>A | ENSP00000316786.5:n.*62C>A | |
NM_000196.3:c.*62C>A | NP_000187.3:n.*62C>A | |
NM_000196.4:c.*62C>A MANE Select | NP_000187.3:n.*62C>A |