Canonical Allele Identifier: CA877129201

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs1398041629
• MyVariant Identifiers: chrX:g.63785320T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785320T>C , CM000685.2:g.63785320T>C	GRCh38
NC_000023.10:g.63005200T>C , CM000685.1:g.63005200T>C	GRCh37
NC_000023.9:g.62921925T>C	NCBI36
NG_016975.1:g.5227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-175A>G	ENSP00000364012.2:n.-175A>G
ENST00000437457.6:c.-175A>G	ENSP00000399994.3:n.-175A>G
ENST00000623417.3:c.-118+10196A>G	ENSP00000485083.1:n.-118+10196A>G
ENST00000623517.3:c.-175A>G	ENSP00000485369.1:n.-175A>G
NM_001173479.1:c.-175A>G	NP_001166950.1:n.-175A>G
XM_005262249.1:c.-175A>G	XP_005262306.1:n.-175A>G
NM_001330495.1:c.-336A>G	NP_001317424.1:n.-336A>G
NM_001353921.1:c.-175A>G	NP_001340850.1:n.-175A>G
NM_001353922.1:c.-175A>G	NP_001340851.1:n.-175A>G
XM_017029378.2:c.-175A>G	XP_016884867.1:n.-175A>G