Canonical Allele Identifier: CA385505356

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158907C>T (hg19) ; chr12:g.57765124C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765124C>T , CM000674.2:g.57765124C>T	GRCh38
NC_000012.11:g.58158907C>T , CM000674.1:g.58158907C>T	GRCh37
NC_000012.10:g.56445174C>T	NCBI36
NG_007076.1:g.7070G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.589G>A
ENST00000713544.1:c.758G>A	ENSP00000518840.1:p.Gly253Asp
ENST00000713545.1:c.735G>A	ENSP00000518841.1:p.Gly245=
ENST00000228606.9:c.677G>A MANE Select	ENSP00000228606.4:p.Gly226Asp
ENST00000228606.8:c.677G>A	ENSP00000228606.4:p.Gly226Asp
ENST00000546567.5:c.-29G>A	ENSP00000449472.1:n.-29G>A
ENST00000546609.1:c.589G>A
ENST00000547344.5:n.816G>A
ENST00000547451.1:n.477G>A
NM_000785.3:c.677G>A	NP_000776.1:p.Gly226Asp
NM_000785.4:c.677G>A MANE Select	NP_000776.1:p.Gly226Asp