Canonical Allele Identifier: CA2038990012

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765652T= , CM000674.2:g.57765652T=	GRCh38
NC_000012.11:g.58159435T= , CM000674.1:g.58159435T=	GRCh37
NC_000012.10:g.56445702T=	NCBI36
NG_007076.1:g.6542A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-153A=
ENST00000713544.1:c.387-72A=	ENSP00000518840.1:n.387-72A=
ENST00000713545.1:c.387-95A=	ENSP00000518841.1:n.387-95A=
ENST00000228606.9:c.387-153A= MANE Select	ENSP00000228606.4:n.387-153A=
ENST00000228606.8:c.387-153A=	ENSP00000228606.4:n.387-153A=
ENST00000546496.1:n.215-153A=
ENST00000546567.5:c.-472A=	ENSP00000449472.1:n.-472A=
ENST00000546609.1:c.299-153A=
ENST00000547344.5:n.441-153A=
ENST00000547451.1:n.34A=
ENST00000552186.1:n.506-153A=
NM_000785.3:c.387-153A=	NP_000776.1:n.387-153A=
NM_000785.4:c.387-153A= MANE Select	NP_000776.1:n.387-153A=