Canonical Allele Identifier: CA2554024
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs756240123
ExAC: 3:119133166 T / A
gnomAD v2: 3-119133166-T-A
gnomAD v3: 3-119414319-T-A
gnomAD v4: 3-119414319-T-A
MyVariant Identifiers: chr3:g.119133166T>A (hg19) chr3:g.119414319T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414319T>A , CM000665.2:g.119414319T>A GRCh38
NC_000003.11:g.119133166T>A , CM000665.1:g.119133166T>A GRCh37
NC_000003.10:g.120615856T>A NCBI36
NG_007665.2:g.124947T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2390T>A MANE Select ENSP00000264245.4:p.Val797Asp
ENST00000264245.8:c.2390T>A ENSP00000264245.4:p.Val797Asp
NM_020754.3:c.2390T>A NP_065805.2:p.Val797Asp
XM_005247671.3:c.2297T>A XP_005247728.1:p.Val766Asp
XM_006713714.2:c.2330T>A XP_006713777.1:p.Val777Asp
XM_006713714.3:c.2330T>A XP_006713777.1:p.Val777Asp
XM_017006955.1:c.1898T>A XP_016862444.1:p.Val633Asp
NM_020754.4:c.2390T>A MANE Select NP_065805.2:p.Val797Asp
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