Canonical Allele Identifier: CA2055289527
Gene:

Linked Data

dbSNP Id: rs1873068247

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293221del , CM000674.2:g.93293221del GRCh38
NC_000012.11:g.93686997del , CM000674.1:g.93686997del GRCh37
NC_000012.10:g.92211128del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34806del