Canonical Allele Identifier: CA1033291929
Gene:

Linked Data

dbSNP Id: rs1672690045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016421_88016425del , CM000664.2:g.88016421_88016425del GRCh38
NC_000002.11:g.88315940_88315944del , CM000664.1:g.88315940_88315944del GRCh37
NC_000002.10:g.88097055_88097059del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.766_770del
XR_940336.3:n.766_770del