Canonical Allele Identifier: CA185736879
Gene: POU5F1B HGNC NCBI
CCAT2 HGNC NCBI
CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1048060109
gnomAD v3: 8-127401328-C-T
gnomAD v4: 8-127401328-C-T
MyVariant Identifiers: chr8:g.128413573C>T (hg19) chr8:g.127401328C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401328C>T , CM000670.2:g.127401328C>T GRCh38
NC_000008.10:g.128413573C>T , CM000670.1:g.128413573C>T GRCh37
NC_000008.9:g.128482755C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13560C>T (POU5F1B) ENSP00000495779.1:n.-559-13560C>T
NR_109834.1:n.930C>T (CCAT2)
NR_117100.1:n.1176+19501G>A (CASC8)
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