Canonical Allele Identifier: CA923857073
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466420A>C , CM000686.2:g.19466420A>C GRCh38
NC_000024.9:g.21628306A>C , CM000686.1:g.21628306A>C GRCh37
NC_000024.8:g.20087694A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+36T>G
ENST00000400605.5:n.1654+36T>G
ENST00000441139.5:n.1671+36T>G
ENST00000513194.1:n.4579+24T>G
NR_002923.2:n.1671+36T>G
NR_033732.1:n.1671+36T>G