Canonical Allele Identifier: CA520110273
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628356A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466470A>C , CM000686.2:g.19466470A>C GRCh38
NC_000024.9:g.21628356A>C , CM000686.1:g.21628356A>C GRCh37
NC_000024.8:g.20087744A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1646T>G
ENST00000400605.5:n.1640T>G
ENST00000441139.5:n.1657T>G
ENST00000513194.1:n.4553T>G
NR_002923.2:n.1657T>G
NR_033732.1:n.1657T>G