Canonical Allele Identifier: CA642213114

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs1462298602
• gnomAD v2: X-63005212-C-G
• gnomAD v3: X-63785332-C-G
• gnomAD v4: X-63785332-C-G
• MyVariant Identifiers: chrX:g.63005212C>G (hg19) ; chrX:g.63785332C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785332C>G , CM000685.2:g.63785332C>G	GRCh38
NC_000023.10:g.63005212C>G , CM000685.1:g.63005212C>G	GRCh37
NC_000023.9:g.62921937C>G	NCBI36
NG_016975.1:g.5215G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-187G>C	ENSP00000364012.2:n.-187G>C
ENST00000437457.6:c.-187G>C	ENSP00000399994.3:n.-187G>C
ENST00000623417.3:c.-118+10184G>C	ENSP00000485083.1:n.-118+10184G>C
ENST00000623517.3:c.-187G>C	ENSP00000485369.1:n.-187G>C
NM_001173479.1:c.-187G>C	NP_001166950.1:n.-187G>C
XM_005262249.1:c.-187G>C	XP_005262306.1:n.-187G>C
NM_001330495.1:c.-348G>C	NP_001317424.1:n.-348G>C
NM_001353921.1:c.-187G>C	NP_001340850.1:n.-187G>C
NM_001353922.1:c.-187G>C	NP_001340851.1:n.-187G>C
XM_017029378.2:c.-187G>C	XP_016884867.1:n.-187G>C