Canonical Allele Identifier: CA540837223

Linked Data

dbSNP Id: rs1203165277
gnomAD v2: 3-8813085-C-G
gnomAD v3: 3-8771399-C-G
gnomAD v4: 3-8771399-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771399C>G , CM000665.2:g.8771399C>G GRCh38
NC_000003.11:g.8813085C>G , CM000665.1:g.8813085C>G GRCh37
NC_000003.10:g.8788085C>G NCBI36
NG_008797.2:g.42590C>G , LRG_329:g.42590C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6078C>G (CAV3)
XM_011533763.1:c.-238-2808G>C (OXTR) XP_011532065.1:n.-238-2808G>C