Canonical Allele Identifier: CA1133627601

Gene: ARHGEF9

Linked Data

• dbSNP Id: rs2056445033
• gnomAD v3: X-63785324-A-G
• gnomAD v4: X-63785324-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.63785324A>G , CM000685.2:g.63785324A>G	GRCh38
NC_000023.10:g.63005204A>G , CM000685.1:g.63005204A>G	GRCh37
NC_000023.9:g.62921929A>G	NCBI36
NG_016975.1:g.5223T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374878.5:c.-179T>C	ENSP00000364012.2:n.-179T>C
ENST00000437457.6:c.-179T>C	ENSP00000399994.3:n.-179T>C
ENST00000623417.3:c.-118+10192T>C	ENSP00000485083.1:n.-118+10192T>C
ENST00000623517.3:c.-179T>C	ENSP00000485369.1:n.-179T>C
NM_001173479.1:c.-179T>C	NP_001166950.1:n.-179T>C
XM_005262249.1:c.-179T>C	XP_005262306.1:n.-179T>C
NM_001330495.1:c.-340T>C	NP_001317424.1:n.-340T>C
NM_001353921.1:c.-179T>C	NP_001340850.1:n.-179T>C
NM_001353922.1:c.-179T>C	NP_001340851.1:n.-179T>C
XM_017029378.2:c.-179T>C	XP_016884867.1:n.-179T>C