Canonical Allele Identifier: CA1473827586
Gene: ARHGAP24 HGNC NCBI
gnomAD v3:
4:85753067 A / G
gnomAD v4:
chr4-85753067-A-G
Joint Max Group AF 0.00007285 (SAS)
Genomes Max Group AF 0.00007285 (SAS)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753067A>G , CM000666.2:g.85753067A>G GRCh38
NC_000004.11:g.86674220A>G , CM000666.1:g.86674220A>G GRCh37
NC_000004.10:g.86893244A>G NCBI36
NG_051627.1:g.282937A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395184.6:c.268+31095A>G MANE Select ENSP00000378611.1:n.268+31095A>G
ENST00000395184.5:c.268+31095A>G ENSP00000378611.1:n.268+31095A>G
ENST00000503995.5:c.268+31095A>G ENSP00000423206.1:n.268+31095A>G
ENST00000512201.5:c.-18+31095A>G ENSP00000426105.1:n.-18+31095A>G
NM_001025616.2:c.268+31095A>G NP_001020787.2:n.268+31095A>G
XM_005263263.3:c.268+31095A>G XP_005263320.1:n.268+31095A>G
XM_024454238.1:c.-18+31095A>G XP_024310006.1:n.-18+31095A>G
XM_024454239.1:c.-18+31095A>G XP_024310007.1:n.-18+31095A>G
NM_001025616.3:c.268+31095A>G MANE Select NP_001020787.2:n.268+31095A>G
Search 100 bp 5'
Search 100 bp 3'