Canonical Allele Identifier: CA717476277
Gene:

Linked Data

dbSNP Id: rs1440665137

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782431del , CM000677.2:g.95782431del GRCh38
NC_000015.9:g.96325660del , CM000677.1:g.96325660del GRCh37
NC_000015.8:g.94126664del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42758del