Canonical Allele Identifier: CA2055289531
Gene:

Linked Data

dbSNP Id: rs1873068341

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293227_93293228del , CM000674.2:g.93293227_93293228del GRCh38
NC_000012.11:g.93687003_93687004del , CM000674.1:g.93687003_93687004del GRCh37
NC_000012.10:g.92211134_92211135del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34800_329+34801del