Canonical Allele Identifier: CA185728722

Linked Data

dbSNP Id: rs77770972

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328667C>G , CM000670.2:g.127328667C>G GRCh38
NC_000008.10:g.128340912C>G , CM000670.1:g.128340912C>G GRCh37
NC_000008.9:g.128410094C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6441C>G (POU5F1B) ENSP00000495779.1:n.-715+6441C>G
NR_117099.1:n.302+6441C>G (CASC21)
NR_117100.1:n.1177-38607G>C (CASC8)