Canonical Allele Identifier: CA2038993856
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57768115G= , CM000674.2:g.57768115G= GRCh38
NC_000012.11:g.58161898G= , CM000674.1:g.58161898G= GRCh37
NC_000012.10:g.56448165G= NCBI36
NG_007076.1:g.4079C=
NG_047060.1:g.9017C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.1:c.107+765C=
ENST00000546609.2:n.107+765C=