Canonical Allele Identifier: CA287548450
Gene:

Linked Data

dbSNP Id: rs200153669

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137248_8137249del , CM000679.2:g.8137248_8137249del GRCh38
NC_000017.10:g.8040566_8040567del , CM000679.1:g.8040566_8040567del GRCh37
NC_000017.9:g.7981291_7981292del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1601_183-1600del
XR_934203.1:n.70-2229_70-2228del
XR_934202.2:n.414-1601_414-1600del