Canonical Allele Identifier: CA2055289529
Gene:

Linked Data

dbSNP Id: rs1873068296

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293224_93293225insAAG , CM000674.2:g.93293224_93293225insAAG GRCh38
NC_000012.11:g.93687000_93687001insAAG , CM000674.1:g.93687000_93687001insAAG GRCh37
NC_000012.10:g.92211131_92211132insAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34802_329+34803insCTT