Canonical Allele Identifier: CA1344418048

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771594G= , CM000665.2:g.8771594G= GRCh38
NC_000003.11:g.8813280G= , CM000665.1:g.8813280G= GRCh37
NC_000003.10:g.8788280G= NCBI36
NG_008797.2:g.42785G= , LRG_329:g.42785G=

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5883G= (CAV3)
XM_011533763.1:c.-238-3003C= (OXTR) XP_011532065.1:n.-238-3003C=