Canonical Allele Identifier: CA1715429978

Gene:

Linked Data

• dbSNP Id: rs1788210070

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69147113del , CM000669.2:g.69147113del	GRCh38
NC_000007.13:g.68612100del , CM000669.1:g.68612100del	GRCh37
NC_000007.12:g.68250036del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927647.1:n.88-987del