Canonical Allele Identifier: CA81697138

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs775575701
• gnomAD v3: 3-119413494-A-T
• gnomAD v4: 3-119413494-A-T
• MyVariant Identifiers: chr3:g.119132341A>T (hg19) ; chr3:g.119413494A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413494A>T , CM000665.2:g.119413494A>T	GRCh38
NC_000003.11:g.119132341A>T , CM000665.1:g.119132341A>T	GRCh37
NC_000003.10:g.120615031A>T	NCBI36
NG_007665.2:g.124122A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-362A>T MANE Select	ENSP00000264245.4:n.1927-362A>T
ENST00000264245.8:c.1927-362A>T	ENSP00000264245.4:n.1927-362A>T
NM_020754.3:c.1927-362A>T	NP_065805.2:n.1927-362A>T
XM_005247671.3:c.1834-362A>T	XP_005247728.1:n.1834-362A>T
XM_006713714.2:c.1867-362A>T	XP_006713777.1:n.1867-362A>T
XM_006713714.3:c.1867-362A>T	XP_006713777.1:n.1867-362A>T
XM_017006955.1:c.1435-362A>T	XP_016862444.1:n.1435-362A>T
NM_020754.4:c.1927-362A>T MANE Select	NP_065805.2:n.1927-362A>T