Canonical Allele Identifier: CA2255111854
Gene:

Linked Data

dbSNP Id: rs1907311371

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237174dup , CM000679.2:g.30237174dup GRCh38
NC_000017.10:g.28564192dup , CM000679.1:g.28564192dup GRCh37
NC_000017.9:g.25588318dup NCBI36
NG_011747.2:g.3763dup

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+104dup
XR_001752824.1:n.280+104dup