Canonical Allele Identifier: CA847111805
Gene:

Linked Data

dbSNP Id: rs1468937812

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999826del , CM000670.2:g.126999826del GRCh38
NC_000008.10:g.128012071del , CM000670.1:g.128012071del GRCh37
NC_000008.9:g.128081253del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6729del