Canonical Allele Identifier: CA963163172
Gene:

Linked Data

dbSNP Id: rs2034712369

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417549del , CM000676.2:g.52417549del GRCh38
NC_000014.8:g.52884267del , CM000676.1:g.52884267del GRCh37
NC_000014.7:g.51954017del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3156del