Canonical Allele Identifier: CA2038987680

Gene: CYP27B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764528G= , CM000674.2:g.57764528G=	GRCh38
NC_000012.11:g.58158311G= , CM000674.1:g.58158311G=	GRCh37
NC_000012.10:g.56444578G=	NCBI36
NG_007076.1:g.7666C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1067C=	ENSP00000518840.1:p.Ala356=
ENST00000713545.1:c.1044C=	ENSP00000518841.1:p.Gly348=
ENST00000228606.9:c.986C= MANE Select	ENSP00000228606.4:p.Ala329=
ENST00000228606.8:c.986C=	ENSP00000228606.4:p.Ala329=
ENST00000546567.5:c.281C=	ENSP00000449472.1:p.Ala94=
ENST00000547344.5:n.1125C=
NM_000785.3:c.986C=	NP_000776.1:p.Ala329=
NM_000785.4:c.986C= MANE Select	NP_000776.1:p.Ala329=