Canonical Allele Identifier: CA1222435242
Gene:

Linked Data

dbSNP Id: rs1659289650

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491641dup , CM000663.2:g.220491641dup GRCh38
NC_000001.10:g.220664983dup , CM000663.1:g.220664983dup GRCh37
NC_000001.9:g.218731606dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-593dup
XR_001737822.1:n.557-593dup