Canonical Allele Identifier: CA2693909219
Gene: ARHGEF9 HGNC NCBI

Linked Data

gnomAD v4: X-63785251-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.63785251C>A , CM000685.2:g.63785251C>A GRCh38
NC_000023.10:g.63005131C>A , CM000685.1:g.63005131C>A GRCh37
NC_000023.9:g.62921856C>A NCBI36
NG_016975.1:g.5296G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374878.5:c.-106G>T ENSP00000364012.2:n.-106G>T
ENST00000437457.6:c.-106G>T ENSP00000399994.3:n.-106G>T
ENST00000623417.3:c.-118+10265G>T ENSP00000485083.1:n.-118+10265G>T
ENST00000623517.3:c.-106G>T ENSP00000485369.1:n.-106G>T
NM_001173479.1:c.-106G>T NP_001166950.1:n.-106G>T
XM_005262249.1:c.-106G>T XP_005262306.1:n.-106G>T
NM_001330495.1:c.-267G>T NP_001317424.1:n.-267G>T
NM_001353921.1:c.-106G>T NP_001340850.1:n.-106G>T
NM_001353922.1:c.-106G>T NP_001340851.1:n.-106G>T
XM_017029378.2:c.-106G>T XP_016884867.1:n.-106G>T