Canonical Allele Identifier: CA520110582
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628424A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466538A>G , CM000686.2:g.19466538A>G GRCh38
NC_000024.9:g.21628424A>G , CM000686.1:g.21628424A>G GRCh37
NC_000024.8:g.20087812A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1578T>C
ENST00000400605.5:n.1572T>C
ENST00000441139.5:n.1589T>C
ENST00000513194.1:n.4485T>C
NR_002923.2:n.1589T>C
NR_033732.1:n.1589T>C
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