Canonical Allele Identifier: CA2554005
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049744
ClinVar RCV Id: RCV001356244
dbSNP Id: rs781272160
ExAC: 3:119133090 G / A
gnomAD v2: 3-119133090-G-A
gnomAD v3: 3-119414243-G-A
gnomAD v4: 3-119414243-G-A
MyVariant Identifiers: chr3:g.119133090G>A (hg19) chr3:g.119414243G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414243G>A , CM000665.2:g.119414243G>A GRCh38
NC_000003.11:g.119133090G>A , CM000665.1:g.119133090G>A GRCh37
NC_000003.10:g.120615780G>A NCBI36
NG_007665.2:g.124871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2314G>A MANE Select ENSP00000264245.4:p.Gly772Arg
ENST00000264245.8:c.2314G>A ENSP00000264245.4:p.Gly772Arg
NM_020754.3:c.2314G>A NP_065805.2:p.Gly772Arg
XM_005247671.3:c.2221G>A XP_005247728.1:p.Gly741Arg
XM_006713714.2:c.2254G>A XP_006713777.1:p.Gly752Arg
XM_006713714.3:c.2254G>A XP_006713777.1:p.Gly752Arg
XM_017006955.1:c.1822G>A XP_016862444.1:p.Gly608Arg
NM_020754.4:c.2314G>A MANE Select NP_065805.2:p.Gly772Arg
Search 100 bp 5'
Search 100 bp 3'