Canonical Allele Identifier: CA1033291646
Gene:

Linked Data

dbSNP Id: rs1672685947

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016356_88016394del , CM000664.2:g.88016356_88016394del GRCh38
NC_000002.11:g.88315875_88315913del , CM000664.1:g.88315875_88315913del GRCh37
NC_000002.10:g.88096990_88097028del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.701_739del
XR_940336.3:n.701_739del