Canonical Allele Identifier: CA435411951

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1411290216
• gnomAD v3: 3-119414317-A-G
• gnomAD v4: 3-119414317-A-G
• MyVariant Identifiers: chr3:g.119133164A>G (hg19) ; chr3:g.119414317A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414317A>G , CM000665.2:g.119414317A>G	GRCh38
NC_000003.11:g.119133164A>G , CM000665.1:g.119133164A>G	GRCh37
NC_000003.10:g.120615854A>G	NCBI36
NG_007665.2:g.124945A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2388A>G MANE Select	ENSP00000264245.4:p.Pro796=
ENST00000264245.8:c.2388A>G	ENSP00000264245.4:p.Pro796=
NM_020754.3:c.2388A>G	NP_065805.2:p.Pro796=
XM_005247671.3:c.2295A>G	XP_005247728.1:p.Pro765=
XM_006713714.2:c.2328A>G	XP_006713777.1:p.Pro776=
XM_006713714.3:c.2328A>G	XP_006713777.1:p.Pro776=
XM_017006955.1:c.1896A>G	XP_016862444.1:p.Pro632=
NM_020754.4:c.2388A>G MANE Select	NP_065805.2:p.Pro796=