Canonical Allele Identifier: CA69856304

Linked Data

dbSNP Id: rs907761421
gnomAD v2: 3-8813275-A-G
gnomAD v3: 3-8771589-A-G
gnomAD v4: 3-8771589-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771589A>G , CM000665.2:g.8771589A>G GRCh38
NC_000003.11:g.8813275A>G , CM000665.1:g.8813275A>G GRCh37
NC_000003.10:g.8788275A>G NCBI36
NG_008797.2:g.42780A>G , LRG_329:g.42780A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5888A>G (CAV3)
XM_011533763.1:c.-238-2998T>C (OXTR) XP_011532065.1:n.-238-2998T>C