Canonical Allele Identifier: CA2703858457

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs2107646424

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413497C>G , CM000665.2:g.119413497C>G	GRCh38
NC_000003.11:g.119132344C>G , CM000665.1:g.119132344C>G	GRCh37
NC_000003.10:g.120615034C>G	NCBI36
NG_007665.2:g.124125C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1927-359C>G MANE Select	ENSP00000264245.4:n.1927-359C>G
ENST00000264245.8:c.1927-359C>G	ENSP00000264245.4:n.1927-359C>G
NM_020754.3:c.1927-359C>G	NP_065805.2:n.1927-359C>G
XM_005247671.3:c.1834-359C>G	XP_005247728.1:n.1834-359C>G
XM_006713714.2:c.1867-359C>G	XP_006713777.1:n.1867-359C>G
XM_006713714.3:c.1867-359C>G	XP_006713777.1:n.1867-359C>G
XM_017006955.1:c.1435-359C>G	XP_016862444.1:n.1435-359C>G
NM_020754.4:c.1927-359C>G MANE Select	NP_065805.2:n.1927-359C>G