Canonical Allele Identifier: CA877129106
Gene: ARHGEF9 HGNC NCBI

Linked Data

dbSNP Id: rs1477910154
gnomAD v3: X-63785223-G-A
gnomAD v4: X-63785223-G-A
MyVariant Identifiers: chrX:g.63785223G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785223G>A , CM000685.2:g.63785223G>A GRCh38
NC_000023.10:g.63005103G>A , CM000685.1:g.63005103G>A GRCh37
NC_000023.9:g.62921828G>A NCBI36
NG_016975.1:g.5324C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374878.5:c.-78C>T ENSP00000364012.2:n.-78C>T
ENST00000437457.6:c.-78C>T ENSP00000399994.3:n.-78C>T
ENST00000623417.3:c.-118+10293C>T ENSP00000485083.1:n.-118+10293C>T
ENST00000623517.3:c.-78C>T ENSP00000485369.1:n.-78C>T
NM_001173479.1:c.-78C>T NP_001166950.1:n.-78C>T
XM_005262249.1:c.-78C>T XP_005262306.1:n.-78C>T
NM_001330495.1:c.-239C>T NP_001317424.1:n.-239C>T
NM_001353921.1:c.-78C>T NP_001340850.1:n.-78C>T
NM_001353922.1:c.-78C>T NP_001340851.1:n.-78C>T
XM_017029378.2:c.-78C>T XP_016884867.1:n.-78C>T