Canonical Allele Identifier: CA69856303

Linked Data

dbSNP Id: rs960909647

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771581T>C , CM000665.2:g.8771581T>C GRCh38
NC_000003.11:g.8813267T>C , CM000665.1:g.8813267T>C GRCh37
NC_000003.10:g.8788267T>C NCBI36
NG_008797.2:g.42772T>C , LRG_329:g.42772T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5896T>C (CAV3)
XM_011533763.1:c.-238-2990A>G (OXTR) XP_011532065.1:n.-238-2990A>G