Canonical Allele Identifier: CA69856309

Linked Data

dbSNP Id: rs991814842
gnomAD v3: 3-8771605-C-A
gnomAD v4: 3-8771605-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771605C>A , CM000665.2:g.8771605C>A GRCh38
NC_000003.11:g.8813291C>A , CM000665.1:g.8813291C>A GRCh37
NC_000003.10:g.8788291C>A NCBI36
NG_008797.2:g.42796C>A , LRG_329:g.42796C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5872C>A (CAV3)
XM_011533763.1:c.-238-3014G>T (OXTR) XP_011532065.1:n.-238-3014G>T