Canonical Allele Identifier: CA2293960328
Gene:

Linked Data

dbSNP Id: rs2031437524

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757074dup , CM000680.2:g.31757074dup GRCh38
NC_000018.9:g.29337037dup , CM000680.1:g.29337037dup GRCh37
NC_000018.8:g.27591035dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5065dup