Canonical Allele Identifier: CA2038991425

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766481T= , CM000674.2:g.57766481T=	GRCh38
NC_000012.11:g.58160264T= , CM000674.1:g.58160264T=	GRCh37
NC_000012.10:g.56446531T=	NCBI36
NG_007076.1:g.5713A=
NG_047060.1:g.10651A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.108-284A=
ENST00000713544.1:c.196-284A=	ENSP00000518840.1:n.196-284A=
ENST00000713545.1:c.196-284A=	ENSP00000518841.1:n.196-284A=
ENST00000228606.9:c.196-284A= MANE Select	ENSP00000228606.4:n.196-284A=
ENST00000228606.8:c.196-284A=	ENSP00000228606.4:n.196-284A=
ENST00000546609.1:c.108-284A=
ENST00000547344.5:n.250-284A=
ENST00000552186.1:n.31A=
NM_000785.3:c.196-284A=	NP_000776.1:n.196-284A=
NM_000785.4:c.196-284A= MANE Select	NP_000776.1:n.196-284A=