Canonical Allele Identifier: CA69856307

Linked Data

dbSNP Id: rs573302326

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771600A>C , CM000665.2:g.8771600A>C GRCh38
NC_000003.11:g.8813286A>C , CM000665.1:g.8813286A>C GRCh37
NC_000003.10:g.8788286A>C NCBI36
NG_008797.2:g.42791A>C , LRG_329:g.42791A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5877A>C (CAV3)
XM_011533763.1:c.-238-3009T>G (OXTR) XP_011532065.1:n.-238-3009T>G