Canonical Allele Identifier: CA1033291138
Gene:

Linked Data

dbSNP Id: rs1672680526

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016271del , CM000664.2:g.88016271del GRCh38
NC_000002.11:g.88315790del , CM000664.1:g.88315790del GRCh37
NC_000002.10:g.88096905del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.616del
XR_940336.3:n.616del