Canonical Allele Identifier: CA1740470109
Gene:

Linked Data

dbSNP Id: rs1795646159

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306340dup , CM000669.2:g.124306340dup GRCh38
NC_000007.13:g.123946394dup , CM000669.1:g.123946394dup GRCh37
NC_000007.12:g.123733630dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-138dup