Canonical Allele Identifier: CA520110764
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628454G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466568G>T , CM000686.2:g.19466568G>T GRCh38
NC_000024.9:g.21628454G>T , CM000686.1:g.21628454G>T GRCh37
NC_000024.8:g.20087842G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1548C>A
ENST00000400605.5:n.1542C>A
ENST00000441139.5:n.1559C>A
ENST00000513194.1:n.4455C>A
NR_002923.2:n.1559C>A
NR_033732.1:n.1559C>A
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