Canonical Allele Identifier: CA435412027

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs776194035
• gnomAD v2: 3-119133188-G-C
• gnomAD v4: 3-119414341-G-C
• MyVariant Identifiers: chr3:g.119133188G>C (hg19) ; chr3:g.119414341G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414341G>C , CM000665.2:g.119414341G>C	GRCh38
NC_000003.11:g.119133188G>C , CM000665.1:g.119133188G>C	GRCh37
NC_000003.10:g.120615878G>C	NCBI36
NG_007665.2:g.124969G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2412G>C MANE Select	ENSP00000264245.4:p.Pro804=
ENST00000264245.8:c.2412G>C	ENSP00000264245.4:p.Pro804=
NM_020754.3:c.2412G>C	NP_065805.2:p.Pro804=
XM_005247671.3:c.2319G>C	XP_005247728.1:p.Pro773=
XM_006713714.2:c.2352G>C	XP_006713777.1:p.Pro784=
XM_006713714.3:c.2352G>C	XP_006713777.1:p.Pro784=
XM_017006955.1:c.1920G>C	XP_016862444.1:p.Pro640=
NM_020754.4:c.2412G>C MANE Select	NP_065805.2:p.Pro804=