Canonical Allele Identifier: CA1481406950
Gene:

Linked Data

dbSNP Id: rs1738955908

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500961_102500966dup , CM000666.2:g.102500961_102500966dup GRCh38
NC_000004.11:g.103422118_103422123dup , CM000666.1:g.103422118_103422123dup GRCh37
NC_000004.10:g.103641150_103641155dup NCBI36
NG_050628.1:g.4633_4638dup

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+286_643+291dup XP_011530769.1:n.643+286_643+291dup
NR_136202.1:n.48+1476_48+1481dup