Canonical Allele Identifier: CA948106554
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs1955356154

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765928dup , CM000674.2:g.57765928dup GRCh38
NC_000012.11:g.58159711dup , CM000674.1:g.58159711dup GRCh37
NC_000012.10:g.56445978dup NCBI36
NG_007076.1:g.6270dup

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.298+83dup
ENST00000713544.1:c.386+83dup ENSP00000518840.1:n.386+83dup
ENST00000713545.1:c.386+83dup ENSP00000518841.1:n.386+83dup
ENST00000228606.9:c.386+83dup MANE Select ENSP00000228606.4:n.386+83dup
ENST00000228606.8:c.386+83dup ENSP00000228606.4:n.386+83dup
ENST00000546496.1:n.214+83dup
ENST00000546609.1:c.298+83dup
ENST00000547344.5:n.440+83dup
ENST00000552186.1:n.505+83dup
NM_000785.3:c.386+83dup NP_000776.1:n.386+83dup
NM_000785.4:c.386+83dup MANE Select NP_000776.1:n.386+83dup