Canonical Allele Identifier: CA642213109

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs1556464583
• gnomAD v2: X-63005184-G-A
• gnomAD v3: X-63785304-G-A
• gnomAD v4: X-63785304-G-A
• MyVariant Identifiers: chrX:g.63005184G>A (hg19) ; chrX:g.63785304G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785304G>A , CM000685.2:g.63785304G>A	GRCh38
NC_000023.10:g.63005184G>A , CM000685.1:g.63005184G>A	GRCh37
NC_000023.9:g.62921909G>A	NCBI36
NG_016975.1:g.5243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-159C>T	ENSP00000364012.2:n.-159C>T
ENST00000437457.6:c.-159C>T	ENSP00000399994.3:n.-159C>T
ENST00000623417.3:c.-118+10212C>T	ENSP00000485083.1:n.-118+10212C>T
ENST00000623517.3:c.-159C>T	ENSP00000485369.1:n.-159C>T
NM_001173479.1:c.-159C>T	NP_001166950.1:n.-159C>T
XM_005262249.1:c.-159C>T	XP_005262306.1:n.-159C>T
NM_001330495.1:c.-320C>T	NP_001317424.1:n.-320C>T
NM_001353921.1:c.-159C>T	NP_001340850.1:n.-159C>T
NM_001353922.1:c.-159C>T	NP_001340851.1:n.-159C>T
XM_017029378.2:c.-159C>T	XP_016884867.1:n.-159C>T