HGVS | Genome Assembly |
---|---|
NC_000015.10:g.58431740G>A , CM000677.2:g.58431740G>A | GRCh38 |
NC_000015.9:g.58723939G>A , CM000677.1:g.58723939G>A | GRCh37 |
NC_000015.8:g.56511231G>A | NCBI36 |
NG_011465.1:g.4765G>A | |
NG_011465.2:g.4765G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356113.10:c.-40-253G>A (LIPC) | ENSP00000348425.6:n.-40-253G>A | |
ENST00000414170.7:c.-40-253G>A (LIPC) | ENSP00000395569.3:n.-40-253G>A | |
ENST00000558239.5:c.-306-11635C>T (ALDH1A2) | ENSP00000453292.1:n.-306-11635C>T | |
ENST00000560257.1:n.564-253G>A (LIPC) | ||
ENST00000560863.5:n.281-11635C>T (ALDH1A2) | ||
XM_005254372.1:c.-40-253G>A (LIPC) | XP_005254429.1:n.-40-253G>A | |
XM_011521551.1:c.-40-253G>A (LIPC) | XP_011519853.1:n.-40-253G>A | |
XM_024449916.1:c.-40-253G>A (LIPC) | XP_024305684.1:n.-40-253G>A | |
XM_024449917.1:c.-77G>A (LIPC) | XP_024305685.1:n.-77G>A |