Canonical Allele Identifier: CA911559056
Gene: CAV3 HGNC NCBI
OXTR HGNC NCBI

Linked Data

dbSNP Id: rs1336313096
gnomAD v3: 3-8771387-A-C
gnomAD v4: 3-8771387-A-C
MyVariant Identifiers: chr3:g.8813073A>C (hg19) chr3:g.8771387A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771387A>C , CM000665.2:g.8771387A>C GRCh38
NC_000003.11:g.8813073A>C , CM000665.1:g.8813073A>C GRCh37
NC_000003.10:g.8788073A>C NCBI36
NG_008797.2:g.42578A>C , LRG_329:g.42578A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6090A>C (CAV3)
XM_011533763.1:c.-238-2796T>G (OXTR) XP_011532065.1:n.-238-2796T>G
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