Canonical Allele Identifier: CA337396496
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1022275411
gnomAD v3: Y-19484678-T-C
gnomAD v4: Y-19484678-T-C
MyVariant Identifiers: chrY:g.21646564T>C (hg19) chrY:g.19484678T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19484678T>C , CM000686.2:g.19484678T>C GRCh38
NC_000024.9:g.21646564T>C , CM000686.1:g.21646564T>C GRCh37
NC_000024.8:g.20105952T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-4384A>G
ENST00000400605.5:n.106-4384A>G
ENST00000441139.5:n.123-4384A>G
ENST00000513194.1:n.207A>G
NR_002923.2:n.123-4384A>G
NR_033732.1:n.123-4384A>G
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