Canonical Allele Identifier: CA385505149

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158808T>A (hg19) ; chr12:g.57765025T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765025T>A , CM000674.2:g.57765025T>A	GRCh38
NC_000012.11:g.58158808T>A , CM000674.1:g.58158808T>A	GRCh37
NC_000012.10:g.56445075T>A	NCBI36
NG_007076.1:g.7169A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.688A>T
ENST00000713544.1:c.857A>T	ENSP00000518840.1:p.Gln286Leu
ENST00000713545.1:c.834A>T	ENSP00000518841.1:p.Pro278=
ENST00000228606.9:c.776A>T MANE Select	ENSP00000228606.4:p.Gln259Leu
ENST00000228606.8:c.776A>T	ENSP00000228606.4:p.Gln259Leu
ENST00000546567.5:c.71A>T	ENSP00000449472.1:p.Gln24Leu
ENST00000546609.1:c.688A>T
ENST00000547344.5:n.915A>T
ENST00000547451.1:n.576A>T
NM_000785.3:c.776A>T	NP_000776.1:p.Gln259Leu
NM_000785.4:c.776A>T MANE Select	NP_000776.1:p.Gln259Leu