Canonical Allele Identifier: CA642213098

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs1256491206
• gnomAD v2: X-63005131-C-T
• gnomAD v3: X-63785251-C-T
• gnomAD v4: X-63785251-C-T
• MyVariant Identifiers: chrX:g.63005131C>T (hg19) ; chrX:g.63785251C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785251C>T , CM000685.2:g.63785251C>T	GRCh38
NC_000023.10:g.63005131C>T , CM000685.1:g.63005131C>T	GRCh37
NC_000023.9:g.62921856C>T	NCBI36
NG_016975.1:g.5296G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374878.5:c.-106G>A	ENSP00000364012.2:n.-106G>A
ENST00000437457.6:c.-106G>A	ENSP00000399994.3:n.-106G>A
ENST00000623417.3:c.-118+10265G>A	ENSP00000485083.1:n.-118+10265G>A
ENST00000623517.3:c.-106G>A	ENSP00000485369.1:n.-106G>A
NM_001173479.1:c.-106G>A	NP_001166950.1:n.-106G>A
XM_005262249.1:c.-106G>A	XP_005262306.1:n.-106G>A
NM_001330495.1:c.-267G>A	NP_001317424.1:n.-267G>A
NM_001353921.1:c.-106G>A	NP_001340850.1:n.-106G>A
NM_001353922.1:c.-106G>A	NP_001340851.1:n.-106G>A
XM_017029378.2:c.-106G>A	XP_016884867.1:n.-106G>A