Canonical Allele Identifier: CA1374121572
Gene:

Linked Data

dbSNP Id: rs1704107127

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266818dup , CM000665.2:g.72266818dup GRCh38
NC_000003.11:g.72315969dup , CM000665.1:g.72315969dup GRCh37
NC_000003.10:g.72398659dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8294dup