Canonical Allele Identifier: CA585063563
Gene: POU5F1B HGNC NCBI
CASC21 HGNC NCBI
CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1336303406
gnomAD v2: 8-128355578-T-C
MyVariant Identifiers: chr8:g.128355578T>C (hg19) chr8:g.127343332T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343332T>C , CM000670.2:g.127343332T>C GRCh38
NC_000008.10:g.128355578T>C , CM000670.1:g.128355578T>C GRCh37
NC_000008.9:g.128424760T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3897T>C (POU5F1B) ENSP00000495779.1:n.-560+3897T>C
NR_117099.1:n.457+3897T>C (CASC21)
NR_117100.1:n.1177-53272A>G (CASC8)
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