Canonical Allele Identifier: CA1804794300
Gene:

Linked Data

dbSNP Id: rs1810399510

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269703dup , CM000670.2:g.97269703dup GRCh38
NC_000008.10:g.98281931dup , CM000670.1:g.98281931dup GRCh37
NC_000008.9:g.98351107dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149367dup