Canonical Allele Identifier: CA1818319474

Linked Data

dbSNP Id: rs1813951892

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328750T>C , CM000670.2:g.127328750T>C GRCh38
NC_000008.10:g.128340995T>C , CM000670.1:g.128340995T>C GRCh37
NC_000008.9:g.128410177T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6524T>C (POU5F1B) ENSP00000495779.1:n.-715+6524T>C
NR_117099.1:n.302+6524T>C (CASC21)
NR_117100.1:n.1177-38690A>G (CASC8)