Canonical Allele Identifier: CA2293960308
Gene:

Linked Data

dbSNP Id: rs2031436945

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757031del , CM000680.2:g.31757031del GRCh38
NC_000018.9:g.29336994del , CM000680.1:g.29336994del GRCh37
NC_000018.8:g.27590992del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5108del