Canonical Allele Identifier: CA2038990038

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765665C= , CM000674.2:g.57765665C=	GRCh38
NC_000012.11:g.58159448C= , CM000674.1:g.58159448C=	GRCh37
NC_000012.10:g.56445715C=	NCBI36
NG_007076.1:g.6529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-166G=
ENST00000713544.1:c.387-85G=	ENSP00000518840.1:n.387-85G=
ENST00000713545.1:c.387-108G=	ENSP00000518841.1:n.387-108G=
ENST00000228606.9:c.387-166G= MANE Select	ENSP00000228606.4:n.387-166G=
ENST00000228606.8:c.387-166G=	ENSP00000228606.4:n.387-166G=
ENST00000546496.1:n.215-166G=
ENST00000546567.5:c.-485G=	ENSP00000449472.1:n.-485G=
ENST00000546609.1:c.299-166G=
ENST00000547344.5:n.441-166G=
ENST00000547451.1:n.21G=
ENST00000552186.1:n.506-166G=
NM_000785.3:c.387-166G=	NP_000776.1:n.387-166G=
NM_000785.4:c.387-166G= MANE Select	NP_000776.1:n.387-166G=