Canonical Allele Identifier: CA385500688

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58157416T>A (hg19) ; chr12:g.57763633T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57763633T>A , CM000674.2:g.57763633T>A	GRCh38
NC_000012.11:g.58157416T>A , CM000674.1:g.58157416T>A	GRCh37
NC_000012.10:g.56443683T>A	NCBI36
NG_007076.1:g.8561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1472A>T	ENSP00000518840.1:p.Glu491Val
ENST00000713545.1:c.*396A>T	ENSP00000518841.1:n.*396A>T
ENST00000228606.9:c.1391A>T MANE Select	ENSP00000228606.4:p.Glu464Val
ENST00000228606.8:c.1391A>T	ENSP00000228606.4:p.Glu464Val
ENST00000547344.5:n.1530A>T
NM_000785.3:c.1391A>T	NP_000776.1:p.Glu464Val
NM_000785.4:c.1391A>T MANE Select	NP_000776.1:p.Glu464Val