Canonical Allele Identifier: CA520110166

Gene: BCORP1

Linked Data

• MyVariant Identifiers: chrY:g.21628337C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19466451C>G , CM000686.2:g.19466451C>G	GRCh38
NC_000024.9:g.21628337C>G , CM000686.1:g.21628337C>G	GRCh37
NC_000024.8:g.20087725C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000650676.1:n.1660+5G>C
ENST00000400605.5:n.1654+5G>C
ENST00000441139.5:n.1671+5G>C
ENST00000513194.1:n.4572G>C
NR_002923.2:n.1671+5G>C
NR_033732.1:n.1671+5G>C