Canonical Allele Identifier: CA1344418051

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771596A= , CM000665.2:g.8771596A= GRCh38
NC_000003.11:g.8813282A= , CM000665.1:g.8813282A= GRCh37
NC_000003.10:g.8788282A= NCBI36
NG_008797.2:g.42787A= , LRG_329:g.42787A=

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5881A= (CAV3)
XM_011533763.1:c.-238-3005T= (OXTR) XP_011532065.1:n.-238-3005T=