Canonical Allele Identifier: CA1344417984

Linked Data

dbSNP Id: rs902701674

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771458C>A , CM000665.2:g.8771458C>A GRCh38
NC_000003.11:g.8813144C>A , CM000665.1:g.8813144C>A GRCh37
NC_000003.10:g.8788144C>A NCBI36
NG_008797.2:g.42649C>A , LRG_329:g.42649C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-6019C>A (CAV3)
XM_011533763.1:c.-238-2867G>T (OXTR) XP_011532065.1:n.-238-2867G>T