Canonical Allele Identifier: CA435411924
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133155G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414308G>A , CM000665.2:g.119414308G>A GRCh38
NC_000003.11:g.119133155G>A , CM000665.1:g.119133155G>A GRCh37
NC_000003.10:g.120615845G>A NCBI36
NG_007665.2:g.124936G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2379G>A MANE Select ENSP00000264245.4:p.Glu793=
ENST00000264245.8:c.2379G>A ENSP00000264245.4:p.Glu793=
NM_020754.3:c.2379G>A NP_065805.2:p.Glu793=
XM_005247671.3:c.2286G>A XP_005247728.1:p.Glu762=
XM_006713714.2:c.2319G>A XP_006713777.1:p.Glu773=
XM_006713714.3:c.2319G>A XP_006713777.1:p.Glu773=
XM_017006955.1:c.1887G>A XP_016862444.1:p.Glu629=
NM_020754.4:c.2379G>A MANE Select NP_065805.2:p.Glu793=
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