HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169549632G>A , CM000663.2:g.169549632G>A | GRCh38 |
NC_000001.10:g.169518870G>A , CM000663.1:g.169518870G>A | GRCh37 |
NC_000001.9:g.167785494G>A | NCBI36 |
NG_011806.1:g.41900C>T , LRG_553:g.41900C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.1611+169C>T MANE Select | ENSP00000356771.3:n.1611+169C>T | |
ENST00000367796.3:c.1611+169C>T | ENSP00000356770.3:n.1611+169C>T | |
ENST00000367797.7:c.1611+169C>T | ENSP00000356771.3:n.1611+169C>T | |
NM_000130.4:c.1611+169C>T , LRG_553t1:c.1611+169C>T | NP_000121.2:n.1611+169C>T | |
XM_017000660.2:c.1200+169C>T | XP_016856149.1:n.1200+169C>T | |
NM_000130.5:c.1611+169C>T MANE Select | NP_000121.2:n.1611+169C>T |