Canonical Allele Identifier: CA2601347930
Gene: ARHGAP24 HGNC NCBI
gnomAD v3:
4:85753063 G / T
gnomAD v4:
chr4-85753063-G-T
Joint Max Group AF 0.00005285 (AMR)
Genomes Max Group AF 0.00005285 (AMR)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753063G>T , CM000666.2:g.85753063G>T GRCh38
NC_000004.11:g.86674216G>T , CM000666.1:g.86674216G>T GRCh37
NC_000004.10:g.86893240G>T NCBI36
NG_051627.1:g.282933G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395184.6:c.268+31091G>T MANE Select ENSP00000378611.1:n.268+31091G>T
ENST00000395184.5:c.268+31091G>T ENSP00000378611.1:n.268+31091G>T
ENST00000503995.5:c.268+31091G>T ENSP00000423206.1:n.268+31091G>T
ENST00000512201.5:c.-18+31091G>T ENSP00000426105.1:n.-18+31091G>T
NM_001025616.2:c.268+31091G>T NP_001020787.2:n.268+31091G>T
XM_005263263.3:c.268+31091G>T XP_005263320.1:n.268+31091G>T
XM_024454238.1:c.-18+31091G>T XP_024310006.1:n.-18+31091G>T
XM_024454239.1:c.-18+31091G>T XP_024310007.1:n.-18+31091G>T
NM_001025616.3:c.268+31091G>T MANE Select NP_001020787.2:n.268+31091G>T
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