Canonical Allele Identifier: CA2206404243
Gene:

Linked Data

dbSNP Id: rs1898216607

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249620dup , CM000678.2:g.9249620dup GRCh38
NC_000016.9:g.9343477dup , CM000678.1:g.9343477dup GRCh37
NC_000016.8:g.9250978dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64887dup