Canonical Allele Identifier: CA847153773

Gene: POU5F1B CCAT2 CASC8

Linked Data

• dbSNP Id: rs897941649
• gnomAD v3: 8-127401164-A-AG
• gnomAD v4: 8-127401164-A-AG
• MyVariant Identifiers: chr8:g.128413409_128413410insG (hg19) ; chr8:g.127401164_127401165insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127401167dup , CM000670.2:g.127401167dup	GRCh38
NC_000008.10:g.128413412dup , CM000670.1:g.128413412dup	GRCh37
NC_000008.9:g.128482594dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645438.1:c.-559-13721dup (POU5F1B)	ENSP00000495779.1:n.-559-13721dup
NR_109834.1:n.769dup (CCAT2)
NR_117100.1:n.1176+19664dup (CASC8)