Canonical Allele Identifier: CA520130696
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1268562979
MyVariant Identifiers: chrY:g.21646718G>A (hg19) chrY:g.19484832G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19484832G>A , CM000686.2:g.19484832G>A GRCh38
NC_000024.9:g.21646718G>A , CM000686.1:g.21646718G>A GRCh37
NC_000024.8:g.20106106G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-4538C>T
ENST00000400605.5:n.106-4538C>T
ENST00000441139.5:n.123-4538C>T
ENST00000513194.1:n.53C>T
NR_002923.2:n.123-4538C>T
NR_033732.1:n.123-4538C>T
Search 100 bp 5'
Search 100 bp 3'