Canonical Allele Identifier: CA385509338
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766140T>G , CM000674.2:g.57766140T>G GRCh38
NC_000012.11:g.58159923T>G , CM000674.1:g.58159923T>G GRCh37
NC_000012.10:g.56446190T>G NCBI36
NG_007076.1:g.6054A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.165A>C
ENST00000713544.1:c.253A>C ENSP00000518840.1:p.Thr85Pro
ENST00000713545.1:c.253A>C ENSP00000518841.1:p.Thr85Pro
ENST00000228606.9:c.253A>C MANE Select ENSP00000228606.4:p.Thr85Pro
ENST00000228606.8:c.253A>C ENSP00000228606.4:p.Thr85Pro
ENST00000546496.1:n.81A>C
ENST00000546609.1:c.165A>C
ENST00000547344.5:n.307A>C
ENST00000552186.1:n.372A>C
NM_000785.3:c.253A>C NP_000776.1:p.Thr85Pro
NM_000785.4:c.253A>C MANE Select NP_000776.1:p.Thr85Pro