Canonical Allele Identifier: CA354051322

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1381549348
• gnomAD v2: 3-119133222-G-C
• gnomAD v4: 3-119414375-G-C
• MyVariant Identifiers: chr3:g.119133222G>C (hg19) ; chr3:g.119414375G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414375G>C , CM000665.2:g.119414375G>C	GRCh38
NC_000003.11:g.119133222G>C , CM000665.1:g.119133222G>C	GRCh37
NC_000003.10:g.120615912G>C	NCBI36
NG_007665.2:g.125003G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2446G>C MANE Select	ENSP00000264245.4:p.Asp816His
ENST00000264245.8:c.2446G>C	ENSP00000264245.4:p.Asp816His
NM_020754.3:c.2446G>C	NP_065805.2:p.Asp816His
XM_005247671.3:c.2353G>C	XP_005247728.1:p.Asp785His
XM_006713714.2:c.2386G>C	XP_006713777.1:p.Asp796His
XM_006713714.3:c.2386G>C	XP_006713777.1:p.Asp796His
XM_017006955.1:c.1954G>C	XP_016862444.1:p.Asp652His
NM_020754.4:c.2446G>C MANE Select	NP_065805.2:p.Asp816His