Canonical Allele Identifier: CA545960929

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs757952631
• gnomAD v2: 3-119132655-A-C
• gnomAD v3: 3-119413808-A-C
• gnomAD v4: 3-119413808-A-C
• MyVariant Identifiers: chr3:g.119132655A>C (hg19) ; chr3:g.119413808A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413808A>C , CM000665.2:g.119413808A>C	GRCh38
NC_000003.11:g.119132655A>C , CM000665.1:g.119132655A>C	GRCh37
NC_000003.10:g.120615345A>C	NCBI36
NG_007665.2:g.124436A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-48A>C MANE Select	ENSP00000264245.4:n.1927-48A>C
ENST00000264245.8:c.1927-48A>C	ENSP00000264245.4:n.1927-48A>C
NM_020754.3:c.1927-48A>C	NP_065805.2:n.1927-48A>C
XM_005247671.3:c.1834-48A>C	XP_005247728.1:n.1834-48A>C
XM_006713714.2:c.1867-48A>C	XP_006713777.1:n.1867-48A>C
XM_006713714.3:c.1867-48A>C	XP_006713777.1:n.1867-48A>C
XM_017006955.1:c.1435-48A>C	XP_016862444.1:n.1435-48A>C
NM_020754.4:c.1927-48A>C MANE Select	NP_065805.2:n.1927-48A>C