Canonical Allele Identifier: CA1344417970

Linked Data

dbSNP Id: rs1708751633

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771438G>A , CM000665.2:g.8771438G>A GRCh38
NC_000003.11:g.8813124G>A , CM000665.1:g.8813124G>A GRCh37
NC_000003.10:g.8788124G>A NCBI36
NG_008797.2:g.42629G>A , LRG_329:g.42629G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6039G>A (CAV3)
XM_011533763.1:c.-238-2847C>T (OXTR) XP_011532065.1:n.-238-2847C>T