Canonical Allele Identifier: CA11620990

Linked Data

dbSNP Id: rs401015
gnomAD v2: 3-8814012-T-C
gnomAD v3: 3-8772326-T-C
gnomAD v4: 3-8772326-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8772326T>C , CM000665.2:g.8772326T>C GRCh38
NC_000003.11:g.8814012T>C , CM000665.1:g.8814012T>C GRCh37
NC_000003.10:g.8789012T>C NCBI36
NG_008797.2:g.43517T>C , LRG_329:g.43517T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-5151T>C (CAV3)
XM_011533763.1:c.-238-3735A>G (OXTR) XP_011532065.1:n.-238-3735A>G