Canonical Allele Identifier: CA520118817
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1603543727
gnomAD v3: Y-19483256-T-G
MyVariant Identifiers: chrY:g.21645142T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483256T>G , CM000686.2:g.19483256T>G GRCh38
NC_000024.9:g.21645142T>G , CM000686.1:g.21645142T>G GRCh37
NC_000024.8:g.20104530T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2962A>C
ENST00000400605.5:n.106-2962A>C
ENST00000441139.5:n.123-2962A>C
ENST00000513194.1:n.1629A>C
NR_002923.2:n.123-2962A>C
NR_033732.1:n.123-2962A>C