Canonical Allele Identifier: CA1344418059

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771605C= , CM000665.2:g.8771605C= GRCh38
NC_000003.11:g.8813291C= , CM000665.1:g.8813291C= GRCh37
NC_000003.10:g.8788291C= NCBI36
NG_008797.2:g.42796C= , LRG_329:g.42796C=

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5872C= (CAV3)
XM_011533763.1:c.-238-3014G= (OXTR) XP_011532065.1:n.-238-3014G=