Canonical Allele Identifier: CA2553950
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs773350526
ExAC: 3:119132802 G / A
gnomAD v2: 3-119132802-G-A
gnomAD v3: 3-119413955-G-A
gnomAD v4: 3-119413955-G-A
MyVariant Identifiers: chr3:g.119132802G>A (hg19) chr3:g.119413955G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413955G>A , CM000665.2:g.119413955G>A GRCh38
NC_000003.11:g.119132802G>A , CM000665.1:g.119132802G>A GRCh37
NC_000003.10:g.120615492G>A NCBI36
NG_007665.2:g.124583G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2026G>A MANE Select ENSP00000264245.4:p.Ala676Thr
ENST00000264245.8:c.2026G>A ENSP00000264245.4:p.Ala676Thr
NM_020754.3:c.2026G>A NP_065805.2:p.Ala676Thr
XM_005247671.3:c.1933G>A XP_005247728.1:p.Ala645Thr
XM_006713714.2:c.1966G>A XP_006713777.1:p.Ala656Thr
XM_006713714.3:c.1966G>A XP_006713777.1:p.Ala656Thr
XM_017006955.1:c.1534G>A XP_016862444.1:p.Ala512Thr
NM_020754.4:c.2026G>A MANE Select NP_065805.2:p.Ala676Thr
Search 100 bp 5'
Search 100 bp 3'