Canonical Allele Identifier: CA276104127
Gene:

Linked Data

dbSNP Id: rs927477530

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782442del , CM000677.2:g.95782442del GRCh38
NC_000015.9:g.96325671del , CM000677.1:g.96325671del GRCh37
NC_000015.8:g.94126675del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42747del