Canonical Allele Identifier: CA2553953
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs754103176
ExAC: 3:119132813 C / G
gnomAD v2: 3-119132813-C-G
gnomAD v4: 3-119413966-C-G
MyVariant Identifiers: chr3:g.119132813C>G (hg19) chr3:g.119413966C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413966C>G , CM000665.2:g.119413966C>G GRCh38
NC_000003.11:g.119132813C>G , CM000665.1:g.119132813C>G GRCh37
NC_000003.10:g.120615503C>G NCBI36
NG_007665.2:g.124594C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2037C>G MANE Select ENSP00000264245.4:p.Thr679=
ENST00000264245.8:c.2037C>G ENSP00000264245.4:p.Thr679=
NM_020754.3:c.2037C>G NP_065805.2:p.Thr679=
XM_005247671.3:c.1944C>G XP_005247728.1:p.Thr648=
XM_006713714.2:c.1977C>G XP_006713777.1:p.Thr659=
XM_006713714.3:c.1977C>G XP_006713777.1:p.Thr659=
XM_017006955.1:c.1545C>G XP_016862444.1:p.Thr515=
NM_020754.4:c.2037C>G MANE Select NP_065805.2:p.Thr679=
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