Canonical Allele Identifier: CA127628860
Gene:

Linked Data

dbSNP Id: rs531161837

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386970dup , CM000667.2:g.129386970dup GRCh38
NC_000005.9:g.128722663dup , CM000667.1:g.128722663dup GRCh37
NC_000005.8:g.128750562dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1478dup
XR_948774.1:n.235-5681dup
XR_001742463.1:n.4089-1478dup
XR_001742464.1:n.2019-5681dup
XR_001742465.1:n.401-1478dup
XR_427770.3:n.337-1478dup