Canonical Allele Identifier: CA354049619
Gene: ARHGAP31 HGNC NCBI

Linked Data

gnomAD v4: 3-119414106-G-A
MyVariant Identifiers: chr3:g.119132953G>A (hg19) chr3:g.119414106G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414106G>A , CM000665.2:g.119414106G>A GRCh38
NC_000003.11:g.119132953G>A , CM000665.1:g.119132953G>A GRCh37
NC_000003.10:g.120615643G>A NCBI36
NG_007665.2:g.124734G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2177G>A MANE Select ENSP00000264245.4:p.Ser726Asn
ENST00000264245.8:c.2177G>A ENSP00000264245.4:p.Ser726Asn
NM_020754.3:c.2177G>A NP_065805.2:p.Ser726Asn
XM_005247671.3:c.2084G>A XP_005247728.1:p.Ser695Asn
XM_006713714.2:c.2117G>A XP_006713777.1:p.Ser706Asn
XM_006713714.3:c.2117G>A XP_006713777.1:p.Ser706Asn
XM_017006955.1:c.1685G>A XP_016862444.1:p.Ser562Asn
NM_020754.4:c.2177G>A MANE Select NP_065805.2:p.Ser726Asn
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