Canonical Allele Identifier: CA1033291028
Gene:

Linked Data

dbSNP Id: rs1672677762

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016234del , CM000664.2:g.88016234del GRCh38
NC_000002.11:g.88315753del , CM000664.1:g.88315753del GRCh37
NC_000002.10:g.88096868del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.579del
XR_940336.3:n.579del