Canonical Allele Identifier: CA354051187
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1377322226
gnomAD v2: 3-119133201-T-C
gnomAD v3: 3-119414354-T-C
gnomAD v4: 3-119414354-T-C
MyVariant Identifiers: chr3:g.119133201T>C (hg19) chr3:g.119414354T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414354T>C , CM000665.2:g.119414354T>C GRCh38
NC_000003.11:g.119133201T>C , CM000665.1:g.119133201T>C GRCh37
NC_000003.10:g.120615891T>C NCBI36
NG_007665.2:g.124982T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2425T>C MANE Select ENSP00000264245.4:p.Ser809Pro
ENST00000264245.8:c.2425T>C ENSP00000264245.4:p.Ser809Pro
NM_020754.3:c.2425T>C NP_065805.2:p.Ser809Pro
XM_005247671.3:c.2332T>C XP_005247728.1:p.Ser778Pro
XM_006713714.2:c.2365T>C XP_006713777.1:p.Ser789Pro
XM_006713714.3:c.2365T>C XP_006713777.1:p.Ser789Pro
XM_017006955.1:c.1933T>C XP_016862444.1:p.Ser645Pro
NM_020754.4:c.2425T>C MANE Select NP_065805.2:p.Ser809Pro
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