Canonical Allele Identifier: CA435412147
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119414398-G-A
MyVariant Identifiers: chr3:g.119133245G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414398G>A , CM000665.2:g.119414398G>A GRCh38
NC_000003.11:g.119133245G>A , CM000665.1:g.119133245G>A GRCh37
NC_000003.10:g.120615935G>A NCBI36
NG_007665.2:g.125026G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2469G>A MANE Select ENSP00000264245.4:p.Lys823=
ENST00000264245.8:c.2469G>A ENSP00000264245.4:p.Lys823=
NM_020754.3:c.2469G>A NP_065805.2:p.Lys823=
XM_005247671.3:c.2376G>A XP_005247728.1:p.Lys792=
XM_006713714.2:c.2409G>A XP_006713777.1:p.Lys803=
XM_006713714.3:c.2409G>A XP_006713777.1:p.Lys803=
XM_017006955.1:c.1977G>A XP_016862444.1:p.Lys659=
NM_020754.4:c.2469G>A MANE Select NP_065805.2:p.Lys823=
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