Canonical Allele Identifier: CA2038989979

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765638G= , CM000674.2:g.57765638G=	GRCh38
NC_000012.11:g.58159421G= , CM000674.1:g.58159421G=	GRCh37
NC_000012.10:g.56445688G=	NCBI36
NG_007076.1:g.6556C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-139C=
ENST00000713544.1:c.387-58C=	ENSP00000518840.1:n.387-58C=
ENST00000713545.1:c.387-81C=	ENSP00000518841.1:n.387-81C=
ENST00000228606.9:c.387-139C= MANE Select	ENSP00000228606.4:n.387-139C=
ENST00000228606.8:c.387-139C=	ENSP00000228606.4:n.387-139C=
ENST00000546496.1:n.215-139C=
ENST00000546567.5:c.-458C=	ENSP00000449472.1:n.-458C=
ENST00000546609.1:c.299-139C=
ENST00000547344.5:n.441-139C=
ENST00000547451.1:n.48C=
ENST00000552186.1:n.506-139C=
NM_000785.3:c.387-139C=	NP_000776.1:n.387-139C=
NM_000785.4:c.387-139C= MANE Select	NP_000776.1:n.387-139C=