Canonical Allele Identifier: CA81697706
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs927299396
MyVariant Identifiers: chr3:g.119133208G>A (hg19) chr3:g.119414361G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414361G>A , CM000665.2:g.119414361G>A GRCh38
NC_000003.11:g.119133208G>A , CM000665.1:g.119133208G>A GRCh37
NC_000003.10:g.120615898G>A NCBI36
NG_007665.2:g.124989G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2432G>A MANE Select ENSP00000264245.4:p.Arg811Lys
ENST00000264245.8:c.2432G>A ENSP00000264245.4:p.Arg811Lys
NM_020754.3:c.2432G>A NP_065805.2:p.Arg811Lys
XM_005247671.3:c.2339G>A XP_005247728.1:p.Arg780Lys
XM_006713714.2:c.2372G>A XP_006713777.1:p.Arg791Lys
XM_006713714.3:c.2372G>A XP_006713777.1:p.Arg791Lys
XM_017006955.1:c.1940G>A XP_016862444.1:p.Arg647Lys
NM_020754.4:c.2432G>A MANE Select NP_065805.2:p.Arg811Lys
Search 100 bp 5'
Search 100 bp 3'