Canonical Allele Identifier: CA1344418397

Linked Data

dbSNP Id: rs401015

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8772326T>G , CM000665.2:g.8772326T>G GRCh38
NC_000003.11:g.8814012T>G , CM000665.1:g.8814012T>G GRCh37
NC_000003.10:g.8789012T>G NCBI36
NG_008797.2:g.43517T>G , LRG_329:g.43517T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-5151T>G (CAV3)
XM_011533763.1:c.-238-3735A>C (OXTR) XP_011532065.1:n.-238-3735A>C