Canonical Allele Identifier: CA385507582

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58159799A>T (hg19) ; chr12:g.57766016A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766016A>T , CM000674.2:g.57766016A>T	GRCh38
NC_000012.11:g.58159799A>T , CM000674.1:g.58159799A>T	GRCh37
NC_000012.10:g.56446066A>T	NCBI36
NG_007076.1:g.6178T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.289T>A
ENST00000713544.1:c.377T>A	ENSP00000518840.1:p.Leu126Gln
ENST00000713545.1:c.377T>A	ENSP00000518841.1:p.Leu126Gln
ENST00000228606.9:c.377T>A MANE Select	ENSP00000228606.4:p.Leu126Gln
ENST00000228606.8:c.377T>A	ENSP00000228606.4:p.Leu126Gln
ENST00000546496.1:n.205T>A
ENST00000546609.1:c.289T>A
ENST00000547344.5:n.431T>A
ENST00000552186.1:n.496T>A
NM_000785.3:c.377T>A	NP_000776.1:p.Leu126Gln
NM_000785.4:c.377T>A MANE Select	NP_000776.1:p.Leu126Gln