Canonical Allele Identifier: CA2554040
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs756470921
ExAC: 3:119133207 A / C
gnomAD v2: 3-119133207-A-C
gnomAD v4: 3-119414360-A-C
MyVariant Identifiers: chr3:g.119133207A>C (hg19) chr3:g.119414360A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414360A>C , CM000665.2:g.119414360A>C GRCh38
NC_000003.11:g.119133207A>C , CM000665.1:g.119133207A>C GRCh37
NC_000003.10:g.120615897A>C NCBI36
NG_007665.2:g.124988A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2431A>C MANE Select ENSP00000264245.4:p.Arg811=
ENST00000264245.8:c.2431A>C ENSP00000264245.4:p.Arg811=
NM_020754.3:c.2431A>C NP_065805.2:p.Arg811=
XM_005247671.3:c.2338A>C XP_005247728.1:p.Arg780=
XM_006713714.2:c.2371A>C XP_006713777.1:p.Arg791=
XM_006713714.3:c.2371A>C XP_006713777.1:p.Arg791=
XM_017006955.1:c.1939A>C XP_016862444.1:p.Arg647=
NM_020754.4:c.2431A>C MANE Select NP_065805.2:p.Arg811=
Search 100 bp 5'
Search 100 bp 3'