Canonical Allele Identifier: CA435411467
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119132807G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413960G>A , CM000665.2:g.119413960G>A GRCh38
NC_000003.11:g.119132807G>A , CM000665.1:g.119132807G>A GRCh37
NC_000003.10:g.120615497G>A NCBI36
NG_007665.2:g.124588G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2031G>A MANE Select ENSP00000264245.4:p.Leu677=
ENST00000264245.8:c.2031G>A ENSP00000264245.4:p.Leu677=
NM_020754.3:c.2031G>A NP_065805.2:p.Leu677=
XM_005247671.3:c.1938G>A XP_005247728.1:p.Leu646=
XM_006713714.2:c.1971G>A XP_006713777.1:p.Leu657=
XM_006713714.3:c.1971G>A XP_006713777.1:p.Leu657=
XM_017006955.1:c.1539G>A XP_016862444.1:p.Leu513=
NM_020754.4:c.2031G>A MANE Select NP_065805.2:p.Leu677=
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