Canonical Allele Identifier: CA101274878

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs943904061
• gnomAD v3: 4-85730216-T-C
• gnomAD v4: 4-85730216-T-C
• MyVariant Identifiers: chr4:g.86651369T>C (hg19) ; chr4:g.85730216T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85730216T>C , CM000666.2:g.85730216T>C	GRCh38
NC_000004.11:g.86651369T>C , CM000666.1:g.86651369T>C	GRCh37
NC_000004.10:g.86870393T>C	NCBI36
NG_051627.1:g.260086T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+8244T>C MANE Select	ENSP00000378611.1:n.268+8244T>C
ENST00000395184.5:c.268+8244T>C	ENSP00000378611.1:n.268+8244T>C
ENST00000503995.5:c.268+8244T>C	ENSP00000423206.1:n.268+8244T>C
ENST00000512201.5:c.-18+8244T>C	ENSP00000426105.1:n.-18+8244T>C
NM_001025616.2:c.268+8244T>C	NP_001020787.2:n.268+8244T>C
XM_005263263.3:c.268+8244T>C	XP_005263320.1:n.268+8244T>C
XM_024454238.1:c.-18+8244T>C	XP_024310006.1:n.-18+8244T>C
XM_024454239.1:c.-18+8244T>C	XP_024310007.1:n.-18+8244T>C
NM_001025616.3:c.268+8244T>C MANE Select	NP_001020787.2:n.268+8244T>C