Canonical Allele Identifier: CA2554036
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs752493947
ExAC: 3:119133194 A / G
gnomAD v2: 3-119133194-A-G
gnomAD v4: 3-119414347-A-G
COSMIC: COSM1240855
MyVariant Identifiers: chr3:g.119133194A>G (hg19) chr3:g.119414347A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414347A>G , CM000665.2:g.119414347A>G GRCh38
NC_000003.11:g.119133194A>G , CM000665.1:g.119133194A>G GRCh37
NC_000003.10:g.120615884A>G NCBI36
NG_007665.2:g.124975A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2418A>G MANE Select ENSP00000264245.4:p.Arg806=
ENST00000264245.8:c.2418A>G ENSP00000264245.4:p.Arg806=
NM_020754.3:c.2418A>G NP_065805.2:p.Arg806=
XM_005247671.3:c.2325A>G XP_005247728.1:p.Arg775=
XM_006713714.2:c.2358A>G XP_006713777.1:p.Arg786=
XM_006713714.3:c.2358A>G XP_006713777.1:p.Arg786=
XM_017006955.1:c.1926A>G XP_016862444.1:p.Arg642=
NM_020754.4:c.2418A>G MANE Select NP_065805.2:p.Arg806=
Search 100 bp 5'
Search 100 bp 3'