HGVS | Genome Assembly |
---|---|
NC_000013.11:g.32315485G>T , CM000675.2:g.32315485G>T | GRCh38 |
NC_000013.10:g.32889622G>T , CM000675.1:g.32889622G>T | GRCh37 |
NC_000013.9:g.31787622G>T | NCBI36 |
NG_012772.3:g.5006G>T , LRG_293:g.5006G>T | |
NG_017006.1:g.1470C>A | |
NG_017006.2:g.4879C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000544455.6:c.-40+340G>T | ENSP00000439902.1:n.-40+340G>T | |
ENST00000380152.7:c.-222G>T | ENSP00000369497.3:n.-222G>T | |
ENST00000544455.5:c.-222G>T | ENSP00000439902.1:n.-222G>T | |
NM_000059.3:c.-222G>T , LRG_293t1:c.-222G>T | NP_000050.2:n.-222G>T | |
XM_011535203.1:c.-40+340G>T | XP_011533505.1:n.-40+340G>T | |
XM_011535204.1:c.-222G>T | XP_011533506.1:n.-222G>T | |
XM_011535205.1:c.-222G>T | XP_011533507.1:n.-222G>T |