Canonical Allele Identifier: CA385505327

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158893A>T (hg19) ; chr12:g.57765110A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765110A>T , CM000674.2:g.57765110A>T	GRCh38
NC_000012.11:g.58158893A>T , CM000674.1:g.58158893A>T	GRCh37
NC_000012.10:g.56445160A>T	NCBI36
NG_007076.1:g.7084T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.603T>A
ENST00000713544.1:c.772T>A	ENSP00000518840.1:p.Ser258Thr
ENST00000713545.1:c.749T>A	ENSP00000518841.1:p.Val250Asp
ENST00000228606.9:c.691T>A MANE Select	ENSP00000228606.4:p.Ser231Thr
ENST00000228606.8:c.691T>A	ENSP00000228606.4:p.Ser231Thr
ENST00000546567.5:c.-15T>A	ENSP00000449472.1:n.-15T>A
ENST00000546609.1:c.603T>A
ENST00000547344.5:n.830T>A
ENST00000547451.1:n.491T>A
NM_000785.3:c.691T>A	NP_000776.1:p.Ser231Thr
NM_000785.4:c.691T>A MANE Select	NP_000776.1:p.Ser231Thr