Canonical Allele Identifier: CA520110544
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628418A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466532A>T , CM000686.2:g.19466532A>T GRCh38
NC_000024.9:g.21628418A>T , CM000686.1:g.21628418A>T GRCh37
NC_000024.8:g.20087806A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1584T>A
ENST00000400605.5:n.1578T>A
ENST00000441139.5:n.1595T>A
ENST00000513194.1:n.4491T>A
NR_002923.2:n.1595T>A
NR_033732.1:n.1595T>A
Search 100 bp 5'
Search 100 bp 3'