Canonical Allele Identifier: CA1267947644
Gene:

Linked Data

dbSNP Id: rs1672689899

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016420dup , CM000664.2:g.88016420dup GRCh38
NC_000002.11:g.88315939dup , CM000664.1:g.88315939dup GRCh37
NC_000002.10:g.88097054dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.765dup
XR_940336.3:n.765dup