Canonical Allele Identifier: CA2755156835

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771382G>C , CM000665.2:g.8771382G>C GRCh38
NC_000003.11:g.8813068G>C , CM000665.1:g.8813068G>C GRCh37
NC_000003.10:g.8788068G>C NCBI36
NG_008797.2:g.42573G>C , LRG_329:g.42573G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000472766.1:n.156-6095G>C (CAV3)
XM_011533763.1:c.-238-2791C>G (OXTR) XP_011532065.1:n.-238-2791C>G