Canonical Allele Identifier: CA2491383696
Gene:

Linked Data

dbSNP Id: rs1664554410

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458391dup , CM000664.2:g.16458391dup GRCh38
NC_000002.11:g.16639659dup , CM000664.1:g.16639659dup GRCh37
NC_000002.10:g.16503140dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3292dup