Canonical Allele Identifier: CA2554030
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 342658
ClinVar RCV Id: RCV000454849 RCV001522002 RCV001554024
dbSNP Id: rs3732413
ExAC: 3:119133183 G / A
gnomAD v2: 3-119133183-G-A
gnomAD v3: 3-119414336-G-A
gnomAD v4: 3-119414336-G-A
MyVariant Identifiers: chr3:g.119133183G>A (hg19) chr3:g.119414336G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414336G>A , CM000665.2:g.119414336G>A GRCh38
NC_000003.11:g.119133183G>A , CM000665.1:g.119133183G>A GRCh37
NC_000003.10:g.120615873G>A NCBI36
NG_007665.2:g.124964G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2407G>A MANE Select ENSP00000264245.4:p.Gly803Ser
ENST00000264245.8:c.2407G>A ENSP00000264245.4:p.Gly803Ser
NM_020754.3:c.2407G>A NP_065805.2:p.Gly803Ser
XM_005247671.3:c.2314G>A XP_005247728.1:p.Gly772Ser
XM_006713714.2:c.2347G>A XP_006713777.1:p.Gly783Ser
XM_006713714.3:c.2347G>A XP_006713777.1:p.Gly783Ser
XM_017006955.1:c.1915G>A XP_016862444.1:p.Gly639Ser
NM_020754.4:c.2407G>A MANE Select NP_065805.2:p.Gly803Ser
Search 100 bp 5'
Search 100 bp 3'