Canonical Allele Identifier: CA2554047
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs560144166
ExAC: 3:119133252 G / A
gnomAD v2: 3-119133252-G-A
gnomAD v3: 3-119414405-G-A
gnomAD v4: 3-119414405-G-A
MyVariant Identifiers: chr3:g.119133252G>A (hg19) chr3:g.119414405G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414405G>A , CM000665.2:g.119414405G>A GRCh38
NC_000003.11:g.119133252G>A , CM000665.1:g.119133252G>A GRCh37
NC_000003.10:g.120615942G>A NCBI36
NG_007665.2:g.125033G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2476G>A MANE Select ENSP00000264245.4:p.Asp826Asn
ENST00000264245.8:c.2476G>A ENSP00000264245.4:p.Asp826Asn
NM_020754.3:c.2476G>A NP_065805.2:p.Asp826Asn
XM_005247671.3:c.2383G>A XP_005247728.1:p.Asp795Asn
XM_006713714.2:c.2416G>A XP_006713777.1:p.Asp806Asn
XM_006713714.3:c.2416G>A XP_006713777.1:p.Asp806Asn
XM_017006955.1:c.1984G>A XP_016862444.1:p.Asp662Asn
NM_020754.4:c.2476G>A MANE Select NP_065805.2:p.Asp826Asn
Search 100 bp 5'
Search 100 bp 3'