Canonical Allele Identifier: CA16603116
Gene: ROCK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376704
ClinVar RCV Id: RCV000424675 RCV000444518
dbSNP Id: rs1057520015
MyVariant Identifiers: chr18:g.18535142G>A (hg19) chr18:g.20955181G>A (hg38)
PubMed: PMID:20140017
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.20955181G>A , CM000680.2:g.20955181G>A GRCh38
NC_000018.9:g.18535142G>A , CM000680.1:g.18535142G>A GRCh37
NC_000018.8:g.16789140G>A NCBI36
NG_042178.2:g.161671C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000635540.2:c.*212C>T ENSP00000489185.1:n.*212C>T
ENST00000399799.3:c.3577C>T MANE Select ENSP00000382697.1:p.Pro1193Ser
ENST00000399799.2:c.3577C>T ENSP00000382697.1:p.Pro1193Ser
ENST00000584687.1:n.287C>T
ENST00000635540.1:c.*212C>T ENSP00000489185.1:n.*212C>T
NM_005406.2:c.3577C>T NP_005397.1:p.Pro1193Ser
XM_011526136.1:c.3655C>T XP_011524438.1:p.Pro1219Ser
XM_011526137.1:c.2188C>T XP_011524439.1:p.Pro730Ser
XM_011526137.3:c.2188C>T XP_011524439.1:p.Pro730Ser
NM_005406.3:c.3577C>T MANE Select NP_005397.1:p.Pro1193Ser
Search 100 bp 5'
Search 100 bp 3'