Canonical Allele Identifier: CA354051673

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1471283030
• gnomAD v3: 3-119414435-G-A
• gnomAD v4: 3-119414435-G-A
• MyVariant Identifiers: chr3:g.119133282G>A (hg19) ; chr3:g.119414435G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414435G>A , CM000665.2:g.119414435G>A	GRCh38
NC_000003.11:g.119133282G>A , CM000665.1:g.119133282G>A	GRCh37
NC_000003.10:g.120615972G>A	NCBI36
NG_007665.2:g.125063G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2506G>A MANE Select	ENSP00000264245.4:p.Gly836Arg
ENST00000264245.8:c.2506G>A	ENSP00000264245.4:p.Gly836Arg
NM_020754.3:c.2506G>A	NP_065805.2:p.Gly836Arg
XM_005247671.3:c.2413G>A	XP_005247728.1:p.Gly805Arg
XM_006713714.2:c.2446G>A	XP_006713777.1:p.Gly816Arg
XM_006713714.3:c.2446G>A	XP_006713777.1:p.Gly816Arg
XM_017006955.1:c.2014G>A	XP_016862444.1:p.Gly672Arg
NM_020754.4:c.2506G>A MANE Select	NP_065805.2:p.Gly836Arg