Canonical Allele Identifier: CA861673965
Gene:

Linked Data

dbSNP Id: rs1359339208

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787380del , CM000671.2:g.1787380del GRCh38
NC_000009.11:g.1787380del , CM000671.1:g.1787380del GRCh37
NC_000009.10:g.1777380del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68468del