HGVS | Genome Assembly |
---|---|
NC_000008.11:g.47960332G>T , CM000670.2:g.47960332G>T | GRCh38 |
NC_000008.10:g.48872892G>T , CM000670.1:g.48872892G>T | GRCh37 |
NC_000008.9:g.49035445G>T | NCBI36 |
NG_023435.1:g.4852C>A , LRG_162:g.4852C>A | |
NG_032967.1:g.5130G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000518221.5:c.-15+12G>T | ENSP00000430329.1:n.-15+12G>T | |
NM_005914.3:c.-813G>T | NP_005905.2:n.-813G>T | |
NM_182746.2:c.-697G>T | NP_877423.1:n.-697G>T | |
XM_005251234.1:c.-1059G>T | XP_005251291.1:n.-1059G>T |