Canonical Allele Identifier: CA526771942
Gene:

Linked Data

dbSNP Id: rs1323315518

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649373dup , CM000663.2:g.168649373dup GRCh38
NC_000001.10:g.168618611dup , CM000663.1:g.168618611dup GRCh37
NC_000001.9:g.166885235dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8097dup
XR_922259.2:n.332-8097dup