Allele Registry

Canonical Allele Identifier: CA11900675

Gene: ARHGAP24 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.85208463T>G

GRCh37 chr4:g.86129616T>G

Linked Data - Sequence & Population

gnomAD v2:

4:86129616 T / G

gnomAD v3:

4:85208463 T / G

gnomAD v4:

chr4-85208463-T-G

Joint Max Group AF 0.47678781 (AFR)

Genomes Max Group AF 0.47678781 (AFR)

Linked Data - NCBI & NCI

dbSNP:

7691216

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

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