Canonical Allele Identifier: CA69856298

Linked Data

dbSNP Id: rs1488467
gnomAD v2: 3-8813231-G-C
gnomAD v3: 3-8771545-G-C
gnomAD v4: 3-8771545-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771545G>C , CM000665.2:g.8771545G>C GRCh38
NC_000003.11:g.8813231G>C , CM000665.1:g.8813231G>C GRCh37
NC_000003.10:g.8788231G>C NCBI36
NG_008797.2:g.42736G>C , LRG_329:g.42736G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5932G>C (CAV3)
XM_011533763.1:c.-238-2954C>G (OXTR) XP_011532065.1:n.-238-2954C>G