Canonical Allele Identifier: CA553019313
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1379748430
gnomAD v2: 4-86674207-G-C
gnomAD v3: 4-85753054-G-C
gnomAD v4: 4-85753054-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753054G>C , CM000666.2:g.85753054G>C GRCh38
NC_000004.11:g.86674207G>C , CM000666.1:g.86674207G>C GRCh37
NC_000004.10:g.86893231G>C NCBI36
NG_051627.1:g.282924G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31082G>C MANE Select ENSP00000378611.1:n.268+31082G>C
ENST00000395184.5:c.268+31082G>C ENSP00000378611.1:n.268+31082G>C
ENST00000503995.5:c.268+31082G>C ENSP00000423206.1:n.268+31082G>C
ENST00000512201.5:c.-18+31082G>C ENSP00000426105.1:n.-18+31082G>C
NM_001025616.2:c.268+31082G>C NP_001020787.2:n.268+31082G>C
XM_005263263.3:c.268+31082G>C XP_005263320.1:n.268+31082G>C
XM_024454238.1:c.-18+31082G>C XP_024310006.1:n.-18+31082G>C
XM_024454239.1:c.-18+31082G>C XP_024310007.1:n.-18+31082G>C
NM_001025616.3:c.268+31082G>C MANE Select NP_001020787.2:n.268+31082G>C