Canonical Allele Identifier: CA1804794133
Gene:

Linked Data

dbSNP Id: rs1810397402

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269575dup , CM000670.2:g.97269575dup GRCh38
NC_000008.10:g.98281803dup , CM000670.1:g.98281803dup GRCh37
NC_000008.9:g.98350979dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149495dup