Canonical Allele Identifier: CA2706508239
Gene:

Linked Data

dbSNP Id: rs28362491

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501002_102501005dup , CM000666.2:g.102501002_102501005dup GRCh38
NC_000004.11:g.103422159_103422162dup , CM000666.1:g.103422159_103422162dup GRCh37
NC_000004.10:g.103641191_103641194dup NCBI36
NG_050628.1:g.4674_4677dup

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+248_643+251dup XP_011530769.1:n.643+248_643+251dup
NR_136202.1:n.48+1438_48+1441dup