Canonical Allele Identifier: CA965992716
Gene:

Linked Data

dbSNP Id: rs1884566675

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307414del , CM000676.2:g.92307414del GRCh38
NC_000014.8:g.92773758del , CM000676.1:g.92773758del GRCh37
NC_000014.7:g.91843511del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2870del