HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119210869A>T , CM000672.2:g.119210869A>T | GRCh38 |
NC_000010.10:g.120970381A>T , CM000672.1:g.120970381A>T | GRCh37 |
NC_000010.9:g.120960371A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392870.3:c.52+2900A>T (GRK5) MANE Select | ENSP00000376609.2:n.52+2900A>T | |
ENST00000392870.2:c.52+2900A>T (GRK5) | ENSP00000376609.2:n.52+2900A>T | |
NM_005308.2:c.52+2900A>T (GRK5) | NP_005299.1:n.52+2900A>T | |
XM_005269707.1:c.52+2900A>T (GRK5) | XP_005269764.1:n.52+2900A>T | |
XM_005269708.1:c.52+2900A>T (GRK5) | XP_005269765.1:n.52+2900A>T | |
XR_246196.2:n.583-612A>T (GRK5-IT1) | ||
XM_005269707.2:c.52+2900A>T (GRK5) | XP_005269764.1:n.52+2900A>T | |
XR_246196.4:n.669-612A>T (GRK5-IT1) | ||
NM_005308.3:c.52+2900A>T (GRK5) MANE Select | NP_005299.1:n.52+2900A>T |