Canonical Allele Identifier: CA923762229
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045110678
gnomAD v3: Y-19562765-T-C
gnomAD v4: Y-19562765-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19562765T>C , CM000686.2:g.19562765T>C GRCh38
NC_000024.9:g.21724651T>C , CM000686.1:g.21724651T>C GRCh37
NC_000024.8:g.20184039T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693243.1:n.26+4217A>G
ENST00000650676.1:n.111+4217A>G
ENST00000651484.1:n.70+4217A>G
XR_938626.1:n.790A>G
XR_938627.1:n.790A>G
XR_938628.1:n.270+4217A>G
XR_938629.1:n.790A>G
XR_001756064.2:n.198+4217A>G
XR_001756065.1:n.198+4217A>G
XR_001756066.1:n.199-3346A>G
XR_938626.2:n.1186A>G
XR_938627.2:n.1186A>G
XR_938628.3:n.198+4217A>G