Canonical Allele Identifier: CA1069062055
Gene:

Linked Data

dbSNP Id: rs1727415669

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601561del , CM000666.2:g.144601561del GRCh38
NC_000004.11:g.145522713del , CM000666.1:g.145522713del GRCh37
NC_000004.10:g.145742163del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185583del ENSP00000497507.1:n.328-185583del