Canonical Allele Identifier: CA385505329

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158895A>T (hg19) ; chr12:g.57765112A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765112A>T , CM000674.2:g.57765112A>T	GRCh38
NC_000012.11:g.58158895A>T , CM000674.1:g.58158895A>T	GRCh37
NC_000012.10:g.56445162A>T	NCBI36
NG_007076.1:g.7082T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.601T>A
ENST00000713544.1:c.770T>A	ENSP00000518840.1:p.Val257Glu
ENST00000713545.1:c.747T>A	ENSP00000518841.1:p.Cys249Ter
ENST00000228606.9:c.689T>A MANE Select	ENSP00000228606.4:p.Val230Glu
ENST00000228606.8:c.689T>A	ENSP00000228606.4:p.Val230Glu
ENST00000546567.5:c.-17T>A	ENSP00000449472.1:n.-17T>A
ENST00000546609.1:c.601T>A
ENST00000547344.5:n.828T>A
ENST00000547451.1:n.489T>A
NM_000785.3:c.689T>A	NP_000776.1:p.Val230Glu
NM_000785.4:c.689T>A MANE Select	NP_000776.1:p.Val230Glu