Canonical Allele Identifier: CA435412076
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133209G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414362G>A , CM000665.2:g.119414362G>A GRCh38
NC_000003.11:g.119133209G>A , CM000665.1:g.119133209G>A GRCh37
NC_000003.10:g.120615899G>A NCBI36
NG_007665.2:g.124990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2433G>A MANE Select ENSP00000264245.4:p.Arg811=
ENST00000264245.8:c.2433G>A ENSP00000264245.4:p.Arg811=
NM_020754.3:c.2433G>A NP_065805.2:p.Arg811=
XM_005247671.3:c.2340G>A XP_005247728.1:p.Arg780=
XM_006713714.2:c.2373G>A XP_006713777.1:p.Arg791=
XM_006713714.3:c.2373G>A XP_006713777.1:p.Arg791=
XM_017006955.1:c.1941G>A XP_016862444.1:p.Arg647=
NM_020754.4:c.2433G>A MANE Select NP_065805.2:p.Arg811=
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