Canonical Allele Identifier: CA911559133

Linked Data

dbSNP Id: rs1225289646

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8771586_8771587del , CM000665.2:g.8771586_8771587del GRCh38
NC_000003.11:g.8813272_8813273del , CM000665.1:g.8813272_8813273del GRCh37
NC_000003.10:g.8788272_8788273del NCBI36
NG_008797.2:g.42777_42778del , LRG_329:g.42777_42778del

Transcript Alleles

HGVS Amino-acid change
ENST00000472766.1:n.156-5891_156-5890del (CAV3)
XM_011533763.1:c.-238-2994_-238-2993del (OXTR) XP_011532065.1:n.-238-2994_-238-2993del