Canonical Allele Identifier: CA799419665

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs971032330
• gnomAD v3: 4-85752786-C-G
• gnomAD v4: 4-85752786-C-G
• MyVariant Identifiers: chr4:g.86673939C>G (hg19) ; chr4:g.85752786C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752786C>G , CM000666.2:g.85752786C>G	GRCh38
NC_000004.11:g.86673939C>G , CM000666.1:g.86673939C>G	GRCh37
NC_000004.10:g.86892963C>G	NCBI36
NG_051627.1:g.282656C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30814C>G MANE Select	ENSP00000378611.1:n.268+30814C>G
ENST00000395184.5:c.268+30814C>G	ENSP00000378611.1:n.268+30814C>G
ENST00000503995.5:c.268+30814C>G	ENSP00000423206.1:n.268+30814C>G
ENST00000512201.5:c.-18+30814C>G	ENSP00000426105.1:n.-18+30814C>G
NM_001025616.2:c.268+30814C>G	NP_001020787.2:n.268+30814C>G
XM_005263263.3:c.268+30814C>G	XP_005263320.1:n.268+30814C>G
XM_024454238.1:c.-18+30814C>G	XP_024310006.1:n.-18+30814C>G
XM_024454239.1:c.-18+30814C>G	XP_024310007.1:n.-18+30814C>G
NM_001025616.3:c.268+30814C>G MANE Select	NP_001020787.2:n.268+30814C>G