Canonical Allele Identifier: CA553019311
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1190570312
gnomAD v2: 4-86674176-G-T
gnomAD v3: 4-85753023-G-T
gnomAD v4: 4-85753023-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753023G>T , CM000666.2:g.85753023G>T GRCh38
NC_000004.11:g.86674176G>T , CM000666.1:g.86674176G>T GRCh37
NC_000004.10:g.86893200G>T NCBI36
NG_051627.1:g.282893G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31051G>T MANE Select ENSP00000378611.1:n.268+31051G>T
ENST00000395184.5:c.268+31051G>T ENSP00000378611.1:n.268+31051G>T
ENST00000503995.5:c.268+31051G>T ENSP00000423206.1:n.268+31051G>T
ENST00000512201.5:c.-18+31051G>T ENSP00000426105.1:n.-18+31051G>T
NM_001025616.2:c.268+31051G>T NP_001020787.2:n.268+31051G>T
XM_005263263.3:c.268+31051G>T XP_005263320.1:n.268+31051G>T
XM_024454238.1:c.-18+31051G>T XP_024310006.1:n.-18+31051G>T
XM_024454239.1:c.-18+31051G>T XP_024310007.1:n.-18+31051G>T
NM_001025616.3:c.268+31051G>T MANE Select NP_001020787.2:n.268+31051G>T