Canonical Allele Identifier: CA1033290780
Gene:

Linked Data

dbSNP Id: rs1672671482

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016043_88016057del , CM000664.2:g.88016043_88016057del GRCh38
NC_000002.11:g.88315562_88315576del , CM000664.1:g.88315562_88315576del GRCh37
NC_000002.10:g.88096677_88096691del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.388_402del
XR_940336.3:n.388_402del