Canonical Allele Identifier: CA2554051
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs113966268
ExAC: 3:119133263 G / T
gnomAD v2: 3-119133263-G-T
gnomAD v3: 3-119414416-G-T
gnomAD v4: 3-119414416-G-T
MyVariant Identifiers: chr3:g.119133263G>T (hg19) chr3:g.119414416G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414416G>T , CM000665.2:g.119414416G>T GRCh38
NC_000003.11:g.119133263G>T , CM000665.1:g.119133263G>T GRCh37
NC_000003.10:g.120615953G>T NCBI36
NG_007665.2:g.125044G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2487G>T MANE Select ENSP00000264245.4:p.Glu829Asp
ENST00000264245.8:c.2487G>T ENSP00000264245.4:p.Glu829Asp
NM_020754.3:c.2487G>T NP_065805.2:p.Glu829Asp
XM_005247671.3:c.2394G>T XP_005247728.1:p.Glu798Asp
XM_006713714.2:c.2427G>T XP_006713777.1:p.Glu809Asp
XM_006713714.3:c.2427G>T XP_006713777.1:p.Glu809Asp
XM_017006955.1:c.1995G>T XP_016862444.1:p.Glu665Asp
NM_020754.4:c.2487G>T MANE Select NP_065805.2:p.Glu829Asp
Search 100 bp 5'
Search 100 bp 3'