Canonical Allele Identifier: CA847155318
Gene: POU5F1B HGNC NCBI
CASC21 HGNC NCBI
CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1423882182
gnomAD v3: 8-127328681-C-T
gnomAD v4: 8-127328681-C-T
MyVariant Identifiers: chr8:g.128340926C>T (hg19) chr8:g.127328681C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328681C>T , CM000670.2:g.127328681C>T GRCh38
NC_000008.10:g.128340926C>T , CM000670.1:g.128340926C>T GRCh37
NC_000008.9:g.128410108C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6455C>T (POU5F1B) ENSP00000495779.1:n.-715+6455C>T
NR_117099.1:n.302+6455C>T (CASC21)
NR_117100.1:n.1177-38621G>A (CASC8)
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