Canonical Allele Identifier: CA2038987758

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764580T= , CM000674.2:g.57764580T=	GRCh38
NC_000012.11:g.58158363T= , CM000674.1:g.58158363T=	GRCh37
NC_000012.10:g.56444630T=	NCBI36
NG_007076.1:g.7614A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1045-30A=	ENSP00000518840.1:n.1045-30A=
ENST00000713545.1:c.1022-30A=	ENSP00000518841.1:n.1022-30A=
ENST00000228606.9:c.964-30A= MANE Select	ENSP00000228606.4:n.964-30A=
ENST00000228606.8:c.964-30A=	ENSP00000228606.4:n.964-30A=
ENST00000546567.5:c.259-30A=	ENSP00000449472.1:n.259-30A=
ENST00000547344.5:n.1103-30A=
ENST00000547451.1:n.937A=
NM_000785.3:c.964-30A=	NP_000776.1:n.964-30A=
NM_000785.4:c.964-30A= MANE Select	NP_000776.1:n.964-30A=