Canonical Allele Identifier: CA2038990969

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766175C= , CM000674.2:g.57766175C=	GRCh38
NC_000012.11:g.58159958C= , CM000674.1:g.58159958C=	GRCh37
NC_000012.10:g.56446225C=	NCBI36
NG_007076.1:g.6019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.130G=
ENST00000713544.1:c.218G=	ENSP00000518840.1:p.Gly73=
ENST00000713545.1:c.218G=	ENSP00000518841.1:p.Gly73=
ENST00000228606.9:c.218G= MANE Select	ENSP00000228606.4:p.Gly73=
ENST00000228606.8:c.218G=	ENSP00000228606.4:p.Gly73=
ENST00000546496.1:n.46G=
ENST00000546609.1:c.130G=
ENST00000547344.5:n.272G=
ENST00000552186.1:n.337G=
NM_000785.3:c.218G=	NP_000776.1:p.Gly73=
NM_000785.4:c.218G= MANE Select	NP_000776.1:p.Gly73=