Canonical Allele Identifier: CA877129194

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs1326695274
• gnomAD v3: X-63785297-G-A
• gnomAD v4: X-63785297-G-A
• MyVariant Identifiers: chrX:g.63785297G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785297G>A , CM000685.2:g.63785297G>A	GRCh38
NC_000023.10:g.63005177G>A , CM000685.1:g.63005177G>A	GRCh37
NC_000023.9:g.62921902G>A	NCBI36
NG_016975.1:g.5250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-152C>T	ENSP00000364012.2:n.-152C>T
ENST00000437457.6:c.-152C>T	ENSP00000399994.3:n.-152C>T
ENST00000623417.3:c.-118+10219C>T	ENSP00000485083.1:n.-118+10219C>T
ENST00000623517.3:c.-152C>T	ENSP00000485369.1:n.-152C>T
NM_001173479.1:c.-152C>T	NP_001166950.1:n.-152C>T
XM_005262249.1:c.-152C>T	XP_005262306.1:n.-152C>T
NM_001330495.1:c.-313C>T	NP_001317424.1:n.-313C>T
NM_001353921.1:c.-152C>T	NP_001340850.1:n.-152C>T
NM_001353922.1:c.-152C>T	NP_001340851.1:n.-152C>T
XM_017029378.2:c.-152C>T	XP_016884867.1:n.-152C>T