Canonical Allele Identifier: CA642213089
Gene: ARHGEF9 HGNC NCBI

Linked Data

dbSNP Id: rs1320652611
gnomAD v2: X-63005043-G-T
gnomAD v4: X-63785163-G-T
MyVariant Identifiers: chrX:g.63005043G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785163G>T , CM000685.2:g.63785163G>T GRCh38
NC_000023.10:g.63005043G>T , CM000685.1:g.63005043G>T GRCh37
NC_000023.9:g.62921768G>T NCBI36
NG_016975.1:g.5384C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000671741.2:c.-18C>A MANE Select ENSP00000500715.1:n.-18C>A
ENST00000672467.1:n.52C>A
ENST00000374878.5:c.-18C>A ENSP00000364012.2:n.-18C>A
ENST00000437457.6:c.-18C>A ENSP00000399994.3:n.-18C>A
ENST00000623417.3:c.-118+10353C>A ENSP00000485083.1:n.-118+10353C>A
ENST00000623517.3:c.-18C>A ENSP00000485369.1:n.-18C>A
ENST00000624355.1:c.-179C>A ENSP00000485327.1:n.-179C>A
ENST00000625116.3:c.-242C>A ENSP00000485160.1:n.-242C>A
NM_001173479.1:c.-18C>A NP_001166950.1:n.-18C>A
XM_005262249.1:c.-18C>A XP_005262306.1:n.-18C>A
XM_005262252.1:c.-179C>A XP_005262309.1:n.-179C>A
NM_001330495.1:c.-179C>A NP_001317424.1:n.-179C>A
NM_001353921.1:c.-18C>A NP_001340850.1:n.-18C>A
NM_001353922.1:c.-18C>A NP_001340851.1:n.-18C>A
XM_017029378.2:c.-18C>A XP_016884867.1:n.-18C>A
XM_024452358.1:c.-179C>A XP_024308126.1:n.-179C>A
NM_001173479.2:c.-18C>A NP_001166950.1:n.-18C>A
NM_001330495.2:c.-179C>A NP_001317424.1:n.-179C>A
NM_001353921.2:c.-18C>A MANE Select NP_001340850.1:n.-18C>A
NM_001353922.2:c.-18C>A NP_001340851.1:n.-18C>A
NM_001369043.1:c.-179C>A NP_001355972.1:n.-179C>A