Canonical Allele Identifier: CA74507197
Gene: RHOA HGNC NCBI

Linked Data

dbSNP Id: rs946125121
gnomAD v3: 3-49359854-T-C
gnomAD v4: 3-49359854-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49359854T>C , CM000665.2:g.49359854T>C GRCh38
NC_000003.11:g.49397287T>C , CM000665.1:g.49397287T>C GRCh37
NC_000003.10:g.49372291T>C NCBI36
NG_012264.1:g.3505A>G
NG_051308.1:g.57244A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000704381.1:c.464+473A>G ENSP00000515884.1:n.464+473A>G
ENST00000418115.6:c.*355A>G MANE Select ENSP00000400175.1:n.*355A>G
ENST00000422781.6:c.*512A>G ENSP00000413587.1:n.*512A>G
ENST00000445425.6:c.*355A>G ENSP00000408402.3:n.*355A>G
ENST00000454011.7:c.*543A>G ENSP00000394483.2:n.*543A>G
ENST00000676712.2:c.*355A>G ENSP00000504603.1:n.*355A>G
ENST00000678200.1:c.*355A>G ENSP00000504180.1:n.*355A>G
ENST00000678921.2:c.*2636A>G ENSP00000503490.1:n.*2636A>G
ENST00000679208.1:c.*355A>G ENSP00000503282.1:n.*355A>G
ENST00000418115.5:c.*355A>G ENSP00000400175.1:n.*355A>G
NM_001313941.1:c.*355A>G NP_001300870.1:n.*355A>G
NM_001313943.1:c.*512A>G NP_001300872.1:n.*512A>G
NM_001313944.1:c.*355A>G NP_001300873.1:n.*355A>G
NM_001313945.1:c.*355A>G NP_001300874.1:n.*355A>G
NM_001313946.1:c.*355A>G NP_001300875.1:n.*355A>G
NM_001313947.1:c.*543A>G NP_001300876.1:n.*543A>G
NM_001664.2:c.*355A>G NP_001655.1:n.*355A>G
NM_001664.3:c.*355A>G NP_001655.1:n.*355A>G
XM_011533695.1:c.*355A>G XP_011531997.1:n.*355A>G
NM_001664.4:c.*355A>G MANE Select NP_001655.1:n.*355A>G
NM_001313941.2:c.*355A>G NP_001300870.1:n.*355A>G
NM_001313943.2:c.*512A>G NP_001300872.1:n.*512A>G
NM_001313944.2:c.*355A>G NP_001300873.1:n.*355A>G
NM_001313945.2:c.*355A>G NP_001300874.1:n.*355A>G
NM_001313946.2:c.*355A>G NP_001300875.1:n.*355A>G
NM_001313947.2:c.*543A>G NP_001300876.1:n.*543A>G