HGVS | Genome Assembly |
---|---|
NC_000019.10:g.11131368G>A , CM000681.2:g.11131368G>A | GRCh38 |
NC_000019.9:g.11242044G>A , CM000681.1:g.11242044G>A | GRCh37 |
NC_000019.8:g.11103044G>A | NCBI36 |
NG_009060.1:g.46988G>A , LRG_274:g.46988G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252444.10:c.*52G>A | ENSP00000252444.6:n.*52G>A | |
ENST00000559340.2:c.*704G>A | ENSP00000453696.2:n.*704G>A | |
ENST00000560467.2:c.*52G>A | ENSP00000453513.2:n.*52G>A | |
ENST00000558518.6:c.*52G>A MANE Select | ENSP00000454071.1:n.*52G>A | |
ENST00000252444.9:c.2889G>A | ||
ENST00000455727.6:c.*52G>A | ENSP00000397829.2:n.*52G>A | |
ENST00000535915.5:c.*52G>A | ENSP00000440520.1:n.*52G>A | |
ENST00000545707.5:c.*52G>A | ENSP00000437639.1:n.*52G>A | |
ENST00000557933.5:c.2697G>A | ENSP00000453557.1:p.Pro899= | |
ENST00000558013.5:c.*52G>A | ENSP00000453346.1:n.*52G>A | |
ENST00000558518.5:c.*52G>A | ENSP00000454071.1:n.*52G>A | |
ENST00000560628.1:n.109-1727G>A | ||
NM_000527.4:c.*52G>A , LRG_274t1:c.*52G>A | NP_000518.1:n.*52G>A | |
NM_001195798.1:c.*52G>A | NP_001182727.1:n.*52G>A | |
NM_001195799.1:c.*52G>A | NP_001182728.1:n.*52G>A | |
NM_001195800.1:c.*52G>A | NP_001182729.1:n.*52G>A | |
NM_001195803.1:c.*52G>A | NP_001182732.1:n.*52G>A | |
XM_011528010.1:c.*52G>A | XP_011526312.1:n.*52G>A | |
XM_011528011.1:c.*52G>A | XP_011526313.1:n.*52G>A | |
XM_011528010.2:c.*52G>A | XP_011526312.1:n.*52G>A | |
XR_001753685.2:n.2969G>A | ||
XR_001753686.2:n.2612G>A | ||
NM_000527.5:c.*52G>A MANE Select | NP_000518.1:n.*52G>A | |
NM_001195798.2:c.*52G>A | NP_001182727.1:n.*52G>A | |
NM_001195799.2:c.*52G>A | NP_001182728.1:n.*52G>A | |
NM_001195800.2:c.*52G>A | NP_001182729.1:n.*52G>A | |
NM_001195803.2:c.*52G>A | NP_001182732.1:n.*52G>A |