Canonical Allele Identifier: CA2705784748
Gene:

Linked Data

dbSNP Id: rs71213077

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557953dup , CM000666.2:g.62557953dup GRCh38
NC_000004.11:g.63423671dup , CM000666.1:g.63423671dup GRCh37
NC_000004.10:g.63106266dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5891dup