Canonical Allele Identifier: CA2038989195

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765279C= , CM000674.2:g.57765279C=	GRCh38
NC_000012.11:g.58159062C= , CM000674.1:g.58159062C=	GRCh37
NC_000012.10:g.56445329C=	NCBI36
NG_007076.1:g.6915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.501+18G=
ENST00000713544.1:c.670+18G=	ENSP00000518840.1:n.670+18G=
ENST00000713545.1:c.647+18G=	ENSP00000518841.1:n.647+18G=
ENST00000228606.9:c.589+18G= MANE Select	ENSP00000228606.4:n.589+18G=
ENST00000228606.8:c.589+18G=	ENSP00000228606.4:n.589+18G=
ENST00000546567.5:c.-117+18G=	ENSP00000449472.1:n.-117+18G=
ENST00000546609.1:c.501+18G=
ENST00000547344.5:n.661G=
ENST00000547451.1:n.389+18G=
NM_000785.3:c.589+18G=	NP_000776.1:n.589+18G=
NM_000785.4:c.589+18G= MANE Select	NP_000776.1:n.589+18G=