Canonical Allele Identifier: CA337395525
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1022200829
gnomAD v3: Y-19460045-T-C
gnomAD v4: Y-19460045-T-C
MyVariant Identifiers: chrY:g.21621931T>C (hg19) chrY:g.19460045T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19460045T>C , CM000686.2:g.19460045T>C GRCh38
NC_000024.9:g.21621931T>C , CM000686.1:g.21621931T>C GRCh37
NC_000024.8:g.20081319T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1842A>G
ENST00000400605.5:n.1836A>G
ENST00000441139.5:n.1794-679A>G
ENST00000513194.1:n.4580-679A>G
NR_002923.2:n.1794-679A>G
NR_033732.1:n.1853A>G
Search 100 bp 5'
Search 100 bp 3'