Canonical Allele Identifier: CA1063282037
Gene:

Linked Data

dbSNP Id: rs1577990845

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557837dup , CM000666.2:g.62557837dup GRCh38
NC_000004.11:g.63423555dup , CM000666.1:g.63423555dup GRCh37
NC_000004.10:g.63106150dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-6007dup