Canonical Allele Identifier: CA11900675
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs7691216
gnomAD v2: 4-86129616-T-G
gnomAD v3: 4-85208463-T-G
gnomAD v4: 4-85208463-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85208463T>G , CM000666.2:g.85208463T>G GRCh38
NC_000004.11:g.86129616T>G , CM000666.1:g.86129616T>G GRCh37
NC_000004.10:g.86348640T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_005263263.3:c.-116-28229T>G XP_005263320.1:n.-116-28229T>G