Canonical Allele Identifier: CA2488911496

Gene: ROCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11268798C= , CM000664.2:g.11268798C=	GRCh38
NC_000002.11:g.11408924C= , CM000664.1:g.11408924C=	GRCh37
NC_000002.10:g.11326375C=	NCBI36
NG_029769.1:g.80788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431087.2:c.183+17741G=	ENSP00000395957.2:n.183+17741G=
ENST00000697752.1:c.324+17741G=	ENSP00000513431.1:n.324+17741G=
ENST00000315872.11:c.324+17741G= MANE Select	ENSP00000317985.6:n.324+17741G=
ENST00000261535.7:c.324+17741G=	ENSP00000261535.3:n.324+17741G=
ENST00000315872.10:c.324+17741G=	ENSP00000317985.6:n.324+17741G=
ENST00000431087.1:c.66+17741G=	ENSP00000395957.1:n.66+17741G=
ENST00000462366.1:n.346+17741G=
ENST00000616279.4:c.-1732+17741G=	ENSP00000481789.1:n.-1732+17741G=
NM_004850.3:c.324+17741G=	NP_004841.2:n.324+17741G=
XM_005246190.3:c.324+17741G=	XP_005246247.1:n.324+17741G=
XM_011510417.1:c.66+17741G=	XP_011508719.1:n.66+17741G=
NM_001321643.1:c.66+17741G=	NP_001308572.1:n.66+17741G=
NM_004850.4:c.324+17741G=	NP_004841.2:n.324+17741G=
XM_011510417.2:c.66+17741G=	XP_011508719.1:n.66+17741G=
XM_017005378.2:c.324+17741G=	XP_016860867.1:n.324+17741G=
XM_017005379.2:c.66+17741G=	XP_016860868.1:n.66+17741G=
NM_004850.5:c.324+17741G= MANE Select	NP_004841.2:n.324+17741G=
NM_001321643.2:c.66+17741G=	NP_001308572.1:n.66+17741G=