Canonical Allele Identifier: CA642213087
Gene: ARHGEF9 HGNC NCBI

Linked Data

dbSNP Id: rs1556464485
gnomAD v2: X-63005033-G-A
gnomAD v3: X-63785153-G-A
gnomAD v4: X-63785153-G-A
MyVariant Identifiers: chrX:g.63005033G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785153G>A , CM000685.2:g.63785153G>A GRCh38
NC_000023.10:g.63005033G>A , CM000685.1:g.63005033G>A GRCh37
NC_000023.9:g.62921758G>A NCBI36
NG_016975.1:g.5394C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.-8C>T MANE Select ENSP00000500715.1:n.-8C>T
ENST00000672467.1:n.62C>T
ENST00000374878.5:c.-8C>T ENSP00000364012.2:n.-8C>T
ENST00000437457.6:c.-8C>T ENSP00000399994.3:n.-8C>T
ENST00000623417.3:c.-118+10363C>T ENSP00000485083.1:n.-118+10363C>T
ENST00000623517.3:c.-8C>T ENSP00000485369.1:n.-8C>T
ENST00000624355.1:c.-169C>T ENSP00000485327.1:n.-169C>T
ENST00000625116.3:c.-232C>T ENSP00000485160.1:n.-232C>T
NM_001173479.1:c.-8C>T NP_001166950.1:n.-8C>T
XM_005262249.1:c.-8C>T XP_005262306.1:n.-8C>T
XM_005262252.1:c.-169C>T XP_005262309.1:n.-169C>T
NM_001330495.1:c.-169C>T NP_001317424.1:n.-169C>T
NM_001353921.1:c.-8C>T NP_001340850.1:n.-8C>T
NM_001353922.1:c.-8C>T NP_001340851.1:n.-8C>T
XM_017029378.2:c.-8C>T XP_016884867.1:n.-8C>T
XM_024452358.1:c.-169C>T XP_024308126.1:n.-169C>T
NM_001173479.2:c.-8C>T NP_001166950.1:n.-8C>T
NM_001330495.2:c.-169C>T NP_001317424.1:n.-169C>T
NM_001353921.2:c.-8C>T MANE Select NP_001340850.1:n.-8C>T
NM_001353922.2:c.-8C>T NP_001340851.1:n.-8C>T
NM_001369043.1:c.-169C>T NP_001355972.1:n.-169C>T