Canonical Allele Identifier: CA755189187
Gene: ROCK2 HGNC NCBI

Linked Data

dbSNP Id: rs943506105
gnomAD v3: 2-11214118-T-C
gnomAD v4: 2-11214118-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11214118T>C , CM000664.2:g.11214118T>C GRCh38
NC_000002.11:g.11354244T>C , CM000664.1:g.11354244T>C GRCh37
NC_000002.10:g.11271695T>C NCBI36
NG_029769.1:g.135468A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697752.1:c.2043+239A>G ENSP00000513431.1:n.2043+239A>G
ENST00000697790.1:c.354+239A>G ENSP00000513442.1:n.354+239A>G
ENST00000697791.1:n.2403+239A>G
ENST00000697792.1:n.2403+239A>G
ENST00000315872.11:c.2043+239A>G MANE Select ENSP00000317985.6:n.2043+239A>G
ENST00000315872.10:c.2043+239A>G ENSP00000317985.6:n.2043+239A>G
ENST00000401753.5:c.1314+239A>G ENSP00000385509.1:n.1314+239A>G
ENST00000616279.4:c.-13+239A>G ENSP00000481789.1:n.-13+239A>G
NM_004850.3:c.2043+239A>G NP_004841.2:n.2043+239A>G
XM_005246190.3:c.2043+239A>G XP_005246247.1:n.2043+239A>G
XM_011510417.1:c.1785+239A>G XP_011508719.1:n.1785+239A>G
NM_001321643.1:c.1785+239A>G NP_001308572.1:n.1785+239A>G
NM_004850.4:c.2043+239A>G NP_004841.2:n.2043+239A>G
XM_011510417.2:c.1785+239A>G XP_011508719.1:n.1785+239A>G
XM_017005378.2:c.2043+239A>G XP_016860867.1:n.2043+239A>G
XM_017005379.2:c.1785+239A>G XP_016860868.1:n.1785+239A>G
NM_004850.5:c.2043+239A>G MANE Select NP_004841.2:n.2043+239A>G
NM_001321643.2:c.1785+239A>G NP_001308572.1:n.1785+239A>G