Canonical Allele Identifier: CA74506865

Gene: RHOA

Linked Data

• dbSNP Id: rs72554687
• gnomAD v2: 3-49396640-T-C
• gnomAD v3: 3-49359207-T-C
• gnomAD v4: 3-49359207-T-C
• MyVariant Identifiers: chr3:g.49396640T>C (hg19) ; chr3:g.49359207T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49359207T>C , CM000665.2:g.49359207T>C	GRCh38
NC_000003.11:g.49396640T>C , CM000665.1:g.49396640T>C	GRCh37
NC_000003.10:g.49371644T>C	NCBI36
NG_012264.1:g.4152A>G
NG_051308.1:g.57891A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704381.1:c.464+1120A>G	ENSP00000515884.1:n.464+1120A>G
ENST00000418115.6:c.*1002A>G MANE Select	ENSP00000400175.1:n.*1002A>G
ENST00000422781.6:c.*1159A>G	ENSP00000413587.1:n.*1159A>G
ENST00000445425.6:c.*1002A>G	ENSP00000408402.3:n.*1002A>G
ENST00000454011.7:c.*1190A>G	ENSP00000394483.2:n.*1190A>G
ENST00000676712.2:c.*1002A>G	ENSP00000504603.1:n.*1002A>G
ENST00000678200.1:c.*1002A>G	ENSP00000504180.1:n.*1002A>G
ENST00000678921.2:c.*3283A>G	ENSP00000503490.1:n.*3283A>G
ENST00000679208.1:c.*1002A>G	ENSP00000503282.1:n.*1002A>G
ENST00000418115.5:c.*1002A>G	ENSP00000400175.1:n.*1002A>G
NM_001313941.1:c.*1002A>G	NP_001300870.1:n.*1002A>G
NM_001313943.1:c.*1159A>G	NP_001300872.1:n.*1159A>G
NM_001313944.1:c.*1002A>G	NP_001300873.1:n.*1002A>G
NM_001313945.1:c.*1002A>G	NP_001300874.1:n.*1002A>G
NM_001313946.1:c.*1002A>G	NP_001300875.1:n.*1002A>G
NM_001313947.1:c.*1190A>G	NP_001300876.1:n.*1190A>G
NM_001664.2:c.*1002A>G	NP_001655.1:n.*1002A>G
NM_001664.3:c.*1002A>G	NP_001655.1:n.*1002A>G
XM_011533695.1:c.*1002A>G	XP_011531997.1:n.*1002A>G
NM_001664.4:c.*1002A>G MANE Select	NP_001655.1:n.*1002A>G
NM_001313941.2:c.*1002A>G	NP_001300870.1:n.*1002A>G
NM_001313943.2:c.*1159A>G	NP_001300872.1:n.*1159A>G
NM_001313944.2:c.*1002A>G	NP_001300873.1:n.*1002A>G
NM_001313945.2:c.*1002A>G	NP_001300874.1:n.*1002A>G
NM_001313946.2:c.*1002A>G	NP_001300875.1:n.*1002A>G
NM_001313947.2:c.*1190A>G	NP_001300876.1:n.*1190A>G