Canonical Allele Identifier: CA1344418079

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771641T= , CM000665.2:g.8771641T= GRCh38
NC_000003.11:g.8813327T= , CM000665.1:g.8813327T= GRCh37
NC_000003.10:g.8788327T= NCBI36
NG_008797.2:g.42832T= , LRG_329:g.42832T=

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5836T= (CAV3)
XM_011533763.1:c.-238-3050A= (OXTR) XP_011532065.1:n.-238-3050A=