Canonical Allele Identifier: CA1344418054

Linked Data

dbSNP Id: rs573302326

Genomic Alleles

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

Transcript Alleles

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