Canonical Allele Identifier: CA42523149

Gene: ROCK2

Linked Data

• dbSNP Id: rs753844974
• MyVariant Identifiers: chr2:g.11354232A>G (hg19) ; chr2:g.11214106A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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