Canonical Allele Identifier: CA11547769

Linked Data

dbSNP Id: rs143825102
gnomAD v2: 3-8813131-G-T
gnomAD v3: 3-8771445-G-T
gnomAD v4: 3-8771445-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771445G>T , CM000665.2:g.8771445G>T GRCh38
NC_000003.11:g.8813131G>T , CM000665.1:g.8813131G>T GRCh37
NC_000003.10:g.8788131G>T NCBI36
NG_008797.2:g.42636G>T , LRG_329:g.42636G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6032G>T (CAV3)
XM_011533763.1:c.-238-2854C>A (OXTR) XP_011532065.1:n.-238-2854C>A