Canonical Allele Identifier: CA69856931

Linked Data

dbSNP Id: rs139832701
gnomAD v2: 3-8814810-T-G
gnomAD v3: 3-8773124-T-G
gnomAD v4: 3-8773124-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8773124T>G , CM000665.2:g.8773124T>G GRCh38
NC_000003.11:g.8814810T>G , CM000665.1:g.8814810T>G GRCh37
NC_000003.10:g.8789810T>G NCBI36
NG_008797.2:g.44315T>G , LRG_329:g.44315T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-4353T>G (CAV3)
XM_011533763.1:c.-238-4533A>C (OXTR) XP_011532065.1:n.-238-4533A>C