Canonical Allele Identifier: CA1344418003

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771503A= , CM000665.2:g.8771503A= GRCh38
NC_000003.11:g.8813189A= , CM000665.1:g.8813189A= GRCh37
NC_000003.10:g.8788189A= NCBI36
NG_008797.2:g.42694A= , LRG_329:g.42694A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-5974A= (CAV3)
XM_011533763.1:c.-238-2912T= (OXTR) XP_011532065.1:n.-238-2912T=