Canonical Allele Identifier: CA553019301
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1166487372
gnomAD v2: 4-86674041-A-G
gnomAD v3: 4-85752888-A-G
gnomAD v4: 4-85752888-A-G
MyVariant Identifiers: chr4:g.86674041A>G (hg19) chr4:g.85752888A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85752888A>G , CM000666.2:g.85752888A>G GRCh38
NC_000004.11:g.86674041A>G , CM000666.1:g.86674041A>G GRCh37
NC_000004.10:g.86893065A>G NCBI36
NG_051627.1:g.282758A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+30916A>G MANE Select ENSP00000378611.1:n.268+30916A>G
ENST00000395184.5:c.268+30916A>G ENSP00000378611.1:n.268+30916A>G
ENST00000503995.5:c.268+30916A>G ENSP00000423206.1:n.268+30916A>G
ENST00000512201.5:c.-18+30916A>G ENSP00000426105.1:n.-18+30916A>G
NM_001025616.2:c.268+30916A>G NP_001020787.2:n.268+30916A>G
XM_005263263.3:c.268+30916A>G XP_005263320.1:n.268+30916A>G
XM_024454238.1:c.-18+30916A>G XP_024310006.1:n.-18+30916A>G
XM_024454239.1:c.-18+30916A>G XP_024310007.1:n.-18+30916A>G
NM_001025616.3:c.268+30916A>G MANE Select NP_001020787.2:n.268+30916A>G
Search 100 bp 5'
Search 100 bp 3'