Canonical Allele Identifier: CA69856301

Linked Data

dbSNP Id: rs923817993
MyVariant Identifiers: chr3:g.8771577T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771577T>A , CM000665.2:g.8771577T>A GRCh38
NC_000003.11:g.8813263T>A , CM000665.1:g.8813263T>A GRCh37
NC_000003.10:g.8788263T>A NCBI36
NG_008797.2:g.42768T>A , LRG_329:g.42768T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5900T>A (CAV3)
XM_011533763.1:c.-238-2986A>T (OXTR) XP_011532065.1:n.-238-2986A>T