Canonical Allele Identifier: CA543891911
Gene:

Linked Data

dbSNP Id: rs56217453

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266864_72266871del , CM000665.2:g.72266864_72266871del GRCh38
NC_000003.11:g.72316015_72316022del , CM000665.1:g.72316015_72316022del GRCh37
NC_000003.10:g.72398705_72398712del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8281_835+8288del