Canonical Allele Identifier: CA1066140472
Gene:

Linked Data

dbSNP Id: rs1738886890

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499868dup , CM000666.2:g.102499868dup GRCh38
NC_000004.11:g.103421025dup , CM000666.1:g.103421025dup GRCh37
NC_000004.10:g.103640057dup NCBI36
NG_050628.1:g.3540dup

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1387dup XP_011530769.1:n.643+1387dup
NR_136202.1:n.48+2577dup