Canonical Allele Identifier: CA520118633
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045064243
gnomAD v3: Y-19483194-C-A
gnomAD v4: Y-19483194-C-A
MyVariant Identifiers: chrY:g.21645080C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483194C>A , CM000686.2:g.19483194C>A GRCh38
NC_000024.9:g.21645080C>A , CM000686.1:g.21645080C>A GRCh37
NC_000024.8:g.20104468C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2900G>T
ENST00000400605.5:n.106-2900G>T
ENST00000441139.5:n.123-2900G>T
ENST00000513194.1:n.1691G>T
NR_002923.2:n.123-2900G>T
NR_033732.1:n.123-2900G>T
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