Canonical Allele Identifier: CA385509308
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766133T>A , CM000674.2:g.57766133T>A GRCh38
NC_000012.11:g.58159916T>A , CM000674.1:g.58159916T>A GRCh37
NC_000012.10:g.56446183T>A NCBI36
NG_007076.1:g.6061A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.172A>T
ENST00000713544.1:c.260A>T ENSP00000518840.1:p.Tyr87Phe
ENST00000713545.1:c.260A>T ENSP00000518841.1:p.Tyr87Phe
ENST00000228606.9:c.260A>T MANE Select ENSP00000228606.4:p.Tyr87Phe
ENST00000228606.8:c.260A>T ENSP00000228606.4:p.Tyr87Phe
ENST00000546496.1:n.88A>T
ENST00000546609.1:c.172A>T
ENST00000547344.5:n.314A>T
ENST00000552186.1:n.379A>T
NM_000785.3:c.260A>T NP_000776.1:p.Tyr87Phe
NM_000785.4:c.260A>T MANE Select NP_000776.1:p.Tyr87Phe