Canonical Allele Identifier: CA435411916
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133266C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414419C>A , CM000665.2:g.119414419C>A GRCh38
NC_000003.11:g.119133266C>A , CM000665.1:g.119133266C>A GRCh37
NC_000003.10:g.120615956C>A NCBI36
NG_007665.2:g.125047C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2490C>A MANE Select ENSP00000264245.4:p.Ile830=
ENST00000264245.8:c.2490C>A ENSP00000264245.4:p.Ile830=
NM_020754.3:c.2490C>A NP_065805.2:p.Ile830=
XM_005247671.3:c.2397C>A XP_005247728.1:p.Ile799=
XM_006713714.2:c.2430C>A XP_006713777.1:p.Ile810=
XM_006713714.3:c.2430C>A XP_006713777.1:p.Ile810=
XM_017006955.1:c.1998C>A XP_016862444.1:p.Ile666=
NM_020754.4:c.2490C>A MANE Select NP_065805.2:p.Ile830=
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