Canonical Allele Identifier: CA540837233

Linked Data

dbSNP Id: rs1377347971
gnomAD v2: 3-8813247-T-A
gnomAD v3: 3-8771561-T-A
gnomAD v4: 3-8771561-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771561T>A , CM000665.2:g.8771561T>A GRCh38
NC_000003.11:g.8813247T>A , CM000665.1:g.8813247T>A GRCh37
NC_000003.10:g.8788247T>A NCBI36
NG_008797.2:g.42752T>A , LRG_329:g.42752T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5916T>A (CAV3)
XM_011533763.1:c.-238-2970A>T (OXTR) XP_011532065.1:n.-238-2970A>T