Canonical Allele Identifier: CA1119008309

Linked Data

dbSNP Id: rs1586442495

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343322T>C , CM000670.2:g.127343322T>C GRCh38
NC_000008.10:g.128355568T>C , CM000670.1:g.128355568T>C GRCh37
NC_000008.9:g.128424750T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+3887T>C (POU5F1B) ENSP00000495779.1:n.-560+3887T>C
NR_117099.1:n.457+3887T>C (CASC21)
NR_117100.1:n.1177-53262A>G (CASC8)