Canonical Allele Identifier: CA15750677
Gene: BCDIN3D-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs10875976

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49832684G>A , CM000674.2:g.49832684G>A GRCh38
NC_000012.11:g.50226467G>A , CM000674.1:g.50226467G>A GRCh37
NC_000012.10:g.48512734G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027499.1:n.355+3601G>A
NR_027500.1:n.351+3601G>A
NR_027501.1:n.351+3601G>A