Canonical Allele Identifier: CA923857076
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466434G>C , CM000686.2:g.19466434G>C GRCh38
NC_000024.9:g.21628320G>C , CM000686.1:g.21628320G>C GRCh37
NC_000024.8:g.20087708G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+22C>G
ENST00000400605.5:n.1654+22C>G
ENST00000441139.5:n.1671+22C>G
ENST00000513194.1:n.4579+10C>G
NR_002923.2:n.1671+22C>G
NR_033732.1:n.1671+22C>G