Canonical Allele Identifier: CA1044893077

Linked Data

dbSNP Id: rs1708753586
gnomAD v3: 3-8771533-C-T
gnomAD v4: 3-8771533-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771533C>T , CM000665.2:g.8771533C>T GRCh38
NC_000003.11:g.8813219C>T , CM000665.1:g.8813219C>T GRCh37
NC_000003.10:g.8788219C>T NCBI36
NG_008797.2:g.42724C>T , LRG_329:g.42724C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5944C>T (CAV3)
XM_011533763.1:c.-238-2942G>A (OXTR) XP_011532065.1:n.-238-2942G>A