Canonical Allele Identifier: CA337396418
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs898914106
gnomAD v3: Y-19483229-G-C
gnomAD v4: Y-19483229-G-C
MyVariant Identifiers: chrY:g.21645115G>C (hg19) chrY:g.19483229G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483229G>C , CM000686.2:g.19483229G>C GRCh38
NC_000024.9:g.21645115G>C , CM000686.1:g.21645115G>C GRCh37
NC_000024.8:g.20104503G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2935C>G
ENST00000400605.5:n.106-2935C>G
ENST00000441139.5:n.123-2935C>G
ENST00000513194.1:n.1656C>G
NR_002923.2:n.123-2935C>G
NR_033732.1:n.123-2935C>G
Search 100 bp 5'
Search 100 bp 3'