Canonical Allele Identifier: CA2488887584
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11214106A= , CM000664.2:g.11214106A= GRCh38
NC_000002.11:g.11354232A= , CM000664.1:g.11354232A= GRCh37
NC_000002.10:g.11271683A= NCBI36
NG_029769.1:g.135480T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697752.1:c.2043+251T= ENSP00000513431.1:n.2043+251T=
ENST00000697790.1:c.354+251T= ENSP00000513442.1:n.354+251T=
ENST00000697791.1:n.2403+251T=
ENST00000697792.1:n.2403+251T=
ENST00000315872.11:c.2043+251T= MANE Select ENSP00000317985.6:n.2043+251T=
ENST00000315872.10:c.2043+251T= ENSP00000317985.6:n.2043+251T=
ENST00000401753.5:c.1314+251T= ENSP00000385509.1:n.1314+251T=
ENST00000616279.4:c.-13+251T= ENSP00000481789.1:n.-13+251T=
NM_004850.3:c.2043+251T= NP_004841.2:n.2043+251T=
XM_005246190.3:c.2043+251T= XP_005246247.1:n.2043+251T=
XM_011510417.1:c.1785+251T= XP_011508719.1:n.1785+251T=
NM_001321643.1:c.1785+251T= NP_001308572.1:n.1785+251T=
NM_004850.4:c.2043+251T= NP_004841.2:n.2043+251T=
XM_011510417.2:c.1785+251T= XP_011508719.1:n.1785+251T=
XM_017005378.2:c.2043+251T= XP_016860867.1:n.2043+251T=
XM_017005379.2:c.1785+251T= XP_016860868.1:n.1785+251T=
NM_004850.5:c.2043+251T= MANE Select NP_004841.2:n.2043+251T=
NM_001321643.2:c.1785+251T= NP_001308572.1:n.1785+251T=