Canonical Allele Identifier: CA2470906499
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1603543907

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512110T>C , CM000686.2:g.19512110T>C GRCh38
NC_000024.9:g.21673996T>C , CM000686.1:g.21673996T>C GRCh37
NC_000024.8:g.20133384T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-31816A>G