Canonical Allele Identifier: CA354051292
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1264683081
gnomAD v2: 3-119133217-G-A
MyVariant Identifiers: chr3:g.119133217G>A (hg19) chr3:g.119414370G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414370G>A , CM000665.2:g.119414370G>A GRCh38
NC_000003.11:g.119133217G>A , CM000665.1:g.119133217G>A GRCh37
NC_000003.10:g.120615907G>A NCBI36
NG_007665.2:g.124998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2441G>A MANE Select ENSP00000264245.4:p.Arg814Lys
ENST00000264245.8:c.2441G>A ENSP00000264245.4:p.Arg814Lys
NM_020754.3:c.2441G>A NP_065805.2:p.Arg814Lys
XM_005247671.3:c.2348G>A XP_005247728.1:p.Arg783Lys
XM_006713714.2:c.2381G>A XP_006713777.1:p.Arg794Lys
XM_006713714.3:c.2381G>A XP_006713777.1:p.Arg794Lys
XM_017006955.1:c.1949G>A XP_016862444.1:p.Arg650Lys
NM_020754.4:c.2441G>A MANE Select NP_065805.2:p.Arg814Lys
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