HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169554931G>A , CM000663.2:g.169554931G>A | GRCh38 |
NC_000001.10:g.169524169G>A , CM000663.1:g.169524169G>A | GRCh37 |
NC_000001.9:g.167790793G>A | NCBI36 |
NG_011806.1:g.36601C>T , LRG_553:g.36601C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1118+251C>T MANE Select | ENSP00000356771.3:n.1118+251C>T | |
ENST00000367796.3:c.1118+251C>T | ENSP00000356770.3:n.1118+251C>T | |
ENST00000367797.7:c.1118+251C>T | ENSP00000356771.3:n.1118+251C>T | |
NM_000130.4:c.1118+251C>T , LRG_553t1:c.1118+251C>T | NP_000121.2:n.1118+251C>T | |
XM_017000660.2:c.707+251C>T | XP_016856149.1:n.707+251C>T | |
NM_000130.5:c.1118+251C>T MANE Select | NP_000121.2:n.1118+251C>T |