Canonical Allele Identifier: CA1344417943

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771367T= , CM000665.2:g.8771367T= GRCh38
NC_000003.11:g.8813053T= , CM000665.1:g.8813053T= GRCh37
NC_000003.10:g.8788053T= NCBI36
NG_008797.2:g.42558T= , LRG_329:g.42558T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6110T= (CAV3)
XM_011533763.1:c.-238-2776A= (OXTR) XP_011532065.1:n.-238-2776A=