HGVS | Genome Assembly |
---|---|
NC_000013.11:g.32315505G>A , CM000675.2:g.32315505G>A | GRCh38 |
NC_000013.10:g.32889642G>A , CM000675.1:g.32889642G>A | GRCh37 |
NC_000013.9:g.31787642G>A | NCBI36 |
NG_012772.3:g.5026G>A , LRG_293:g.5026G>A | |
NG_017006.1:g.1450C>T | |
NG_017006.2:g.4859C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000530893.7:c.-567G>A | ENSP00000499438.2:n.-567G>A | |
ENST00000544455.6:c.-40+360G>A | ENSP00000439902.1:n.-40+360G>A | |
ENST00000380152.7:c.-202G>A | ENSP00000369497.3:n.-202G>A | |
ENST00000530893.6:n.1G>A | ||
ENST00000544455.5:c.-202G>A | ENSP00000439902.1:n.-202G>A | |
NM_000059.3:c.-202G>A , LRG_293t1:c.-202G>A | NP_000050.2:n.-202G>A | |
XM_011535203.1:c.-40+360G>A | XP_011533505.1:n.-40+360G>A | |
XM_011535204.1:c.-202G>A | XP_011533506.1:n.-202G>A | |
XM_011535205.1:c.-202G>A | XP_011533507.1:n.-202G>A |