Canonical Allele Identifier: CA1044893083

Linked Data

dbSNP Id: rs1708754119
gnomAD v3: 3-8771547-A-G
gnomAD v4: 3-8771547-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771547A>G , CM000665.2:g.8771547A>G GRCh38
NC_000003.11:g.8813233A>G , CM000665.1:g.8813233A>G GRCh37
NC_000003.10:g.8788233A>G NCBI36
NG_008797.2:g.42738A>G , LRG_329:g.42738A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5930A>G (CAV3)
XM_011533763.1:c.-238-2956T>C (OXTR) XP_011532065.1:n.-238-2956T>C