Canonical Allele Identifier: CA727900865
Gene:

Linked Data

dbSNP Id: rs1477523454

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237214dup , CM000679.2:g.30237214dup GRCh38
NC_000017.10:g.28564232dup , CM000679.1:g.28564232dup GRCh37
NC_000017.9:g.25588358dup NCBI36
NG_011747.2:g.3728dup

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+144dup
XR_001752824.1:n.280+144dup