Canonical Allele Identifier: CA585063560

Linked Data

dbSNP Id: rs34796978

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343310_127343315dup , CM000670.2:g.127343310_127343315dup GRCh38
NC_000008.10:g.128355556_128355561dup , CM000670.1:g.128355556_128355561dup GRCh37
NC_000008.9:g.128424738_128424743dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3875_-560+3880dup (POU5F1B) ENSP00000495779.1:n.-560+3875_-560+3880dup
NR_117099.1:n.457+3875_457+3880dup (CASC21)
NR_117100.1:n.1177-53251_1177-53246dup (CASC8)