Canonical Allele Identifier: CA2693909220
Gene: ARHGEF9 HGNC NCBI

Linked Data

gnomAD v4: X-63785252-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785252C>T , CM000685.2:g.63785252C>T GRCh38
NC_000023.10:g.63005132C>T , CM000685.1:g.63005132C>T GRCh37
NC_000023.9:g.62921857C>T NCBI36
NG_016975.1:g.5295G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374878.5:c.-107G>A ENSP00000364012.2:n.-107G>A
ENST00000437457.6:c.-107G>A ENSP00000399994.3:n.-107G>A
ENST00000623417.3:c.-118+10264G>A ENSP00000485083.1:n.-118+10264G>A
ENST00000623517.3:c.-107G>A ENSP00000485369.1:n.-107G>A
NM_001173479.1:c.-107G>A NP_001166950.1:n.-107G>A
XM_005262249.1:c.-107G>A XP_005262306.1:n.-107G>A
NM_001330495.1:c.-268G>A NP_001317424.1:n.-268G>A
NM_001353921.1:c.-107G>A NP_001340850.1:n.-107G>A
NM_001353922.1:c.-107G>A NP_001340851.1:n.-107G>A
XM_017029378.2:c.-107G>A XP_016884867.1:n.-107G>A
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