Canonical Allele Identifier: CA352786786

Gene: RHOA

Linked Data

• ClinVar Variation Id: 521191
• ClinVar RCV Id: RCV000623047
• dbSNP Id: rs1553631976
• MyVariant Identifiers: chr3:g.49405942A>G (hg19) ; chr3:g.49368509A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49368509A>G , CM000665.2:g.49368509A>G	GRCh38
NC_000003.11:g.49405942A>G , CM000665.1:g.49405942A>G	GRCh37
NC_000003.10:g.49380946A>G	NCBI36
NG_051308.1:g.48589T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704381.1:c.196T>C	ENSP00000515884.1:p.Tyr66His
ENST00000418115.6:c.196T>C MANE Select	ENSP00000400175.1:p.Tyr66His
ENST00000422781.6:c.196T>C	ENSP00000413587.1:p.Tyr66His
ENST00000445425.6:c.196T>C	ENSP00000408402.3:p.Tyr66His
ENST00000454011.7:c.157-5883T>C	ENSP00000394483.2:n.157-5883T>C
ENST00000676712.2:c.156+6925T>C	ENSP00000504603.1:n.156+6925T>C
ENST00000677684.1:c.194T>C	ENSP00000504494.1:p.Leu65Ser
ENST00000678200.1:c.196T>C	ENSP00000504180.1:p.Tyr66His
ENST00000678921.2:c.196T>C	ENSP00000503490.1:p.Tyr66His
ENST00000679208.1:c.196T>C	ENSP00000503282.1:p.Tyr66His
ENST00000418115.5:c.196T>C	ENSP00000400175.1:p.Tyr66His
ENST00000422781.5:c.196T>C	ENSP00000413587.1:p.Tyr66His
ENST00000445425.4:c.196T>C	ENSP00000408402.1:p.Tyr66His
ENST00000454011.6:c.157-5883T>C	ENSP00000394483.2:n.157-5883T>C
NM_001313941.1:c.196T>C	NP_001300870.1:p.Tyr66His
NM_001313943.1:c.196T>C	NP_001300872.1:p.Tyr66His
NM_001313944.1:c.136T>C	NP_001300873.1:p.Tyr46His
NM_001313945.1:c.-48T>C	NP_001300874.1:n.-48T>C
NM_001313946.1:c.156+6925T>C	NP_001300875.1:n.156+6925T>C
NM_001313947.1:c.157-5883T>C	NP_001300876.1:n.157-5883T>C
NM_001664.2:c.196T>C	NP_001655.1:p.Tyr66His
NM_001664.3:c.196T>C	NP_001655.1:p.Tyr66His
XM_011533695.1:c.196T>C	XP_011531997.1:p.Tyr66His
NM_001664.4:c.196T>C MANE Select	NP_001655.1:p.Tyr66His
NM_001313941.2:c.196T>C	NP_001300870.1:p.Tyr66His
NM_001313943.2:c.196T>C	NP_001300872.1:p.Tyr66His
NM_001313944.2:c.136T>C	NP_001300873.1:p.Tyr46His
NM_001313945.2:c.-48T>C	NP_001300874.1:n.-48T>C
NM_001313946.2:c.156+6925T>C	NP_001300875.1:n.156+6925T>C
NM_001313947.2:c.157-5883T>C	NP_001300876.1:n.157-5883T>C