Canonical Allele Identifier: CA923857148
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045047215
gnomAD v3: Y-19466756-T-C
gnomAD v4: Y-19466756-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466756T>C , CM000686.2:g.19466756T>C GRCh38
NC_000024.9:g.21628642T>C , CM000686.1:g.21628642T>C GRCh37
NC_000024.8:g.20088030T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1360A>G
ENST00000400605.5:n.1354A>G
ENST00000441139.5:n.1371A>G
ENST00000513194.1:n.4316-49A>G
NR_002923.2:n.1371A>G
NR_033732.1:n.1371A>G