HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665244A>T , CM000679.2:g.39665244A>T | GRCh38 |
NC_000017.10:g.37821497A>T , CM000679.1:g.37821497A>T | GRCh37 |
NC_000017.9:g.35075023A>T | NCBI36 |
NG_008892.1:g.4899A>T , LRG_210:g.4899A>T | |
NG_042278.1:g.2264A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.2:c.-116A>T | ENSP00000312624.2:n.-116A>T |