Canonical Allele Identifier: CA520118348
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644984T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483098T>C , CM000686.2:g.19483098T>C GRCh38
NC_000024.9:g.21644984T>C , CM000686.1:g.21644984T>C GRCh37
NC_000024.8:g.20104372T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2804A>G
ENST00000400605.5:n.106-2804A>G
ENST00000441139.5:n.123-2804A>G
ENST00000513194.1:n.1787A>G
NR_002923.2:n.123-2804A>G
NR_033732.1:n.123-2804A>G