Canonical Allele Identifier: CA354049574

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1264560025
• gnomAD v4: 3-119414100-A-G
• MyVariant Identifiers: chr3:g.119132947A>G (hg19) ; chr3:g.119414100A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414100A>G , CM000665.2:g.119414100A>G	GRCh38
NC_000003.11:g.119132947A>G , CM000665.1:g.119132947A>G	GRCh37
NC_000003.10:g.120615637A>G	NCBI36
NG_007665.2:g.124728A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2171A>G MANE Select	ENSP00000264245.4:p.Asn724Ser
ENST00000264245.8:c.2171A>G	ENSP00000264245.4:p.Asn724Ser
NM_020754.3:c.2171A>G	NP_065805.2:p.Asn724Ser
XM_005247671.3:c.2078A>G	XP_005247728.1:p.Asn693Ser
XM_006713714.2:c.2111A>G	XP_006713777.1:p.Asn704Ser
XM_006713714.3:c.2111A>G	XP_006713777.1:p.Asn704Ser
XM_017006955.1:c.1679A>G	XP_016862444.1:p.Asn560Ser
NM_020754.4:c.2171A>G MANE Select	NP_065805.2:p.Asn724Ser