Canonical Allele Identifier: CA520110175
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628339C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466453C>T , CM000686.2:g.19466453C>T GRCh38
NC_000024.9:g.21628339C>T , CM000686.1:g.21628339C>T GRCh37
NC_000024.8:g.20087727C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+3G>A
ENST00000400605.5:n.1654+3G>A
ENST00000441139.5:n.1671+3G>A
ENST00000513194.1:n.4570G>A
NR_002923.2:n.1671+3G>A
NR_033732.1:n.1671+3G>A