Canonical Allele Identifier: CA2038994140
Community Standard Title: NC_000012.12:g.57768302G=
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57768302G= , CM000674.2:g.57768302G= GRCh38
NC_000012.11:g.58162085G= , CM000674.1:g.58162085G= GRCh37
NC_000012.10:g.56448352G= NCBI36
NG_007076.1:g.3892C=
NG_047060.1:g.8830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.1:c.107+578C=
ENST00000546609.2:n.107+578C=