Canonical Allele Identifier: CA1038177566
Gene:

Linked Data

dbSNP Id: rs1683148679

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870603dup , CM000664.2:g.155870603dup GRCh38
NC_000002.11:g.156727115dup , CM000664.1:g.156727115dup GRCh37
NC_000002.10:g.156435361dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3416dup
XR_001739749.1:n.331-29619dup
XR_001739750.1:n.331-29619dup
XR_001739751.1:n.331-29619dup
XR_923501.2:n.331-3416dup