Canonical Allele Identifier: CA385503422
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764421A>T , CM000674.2:g.57764421A>T GRCh38
NC_000012.11:g.58158204A>T , CM000674.1:g.58158204A>T GRCh37
NC_000012.10:g.56444471A>T NCBI36
NG_007076.1:g.7773T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1174T>A ENSP00000518840.1:p.Ser392Thr
ENST00000713545.1:c.*98T>A ENSP00000518841.1:n.*98T>A
ENST00000228606.9:c.1093T>A MANE Select ENSP00000228606.4:p.Ser365Thr
ENST00000228606.8:c.1093T>A ENSP00000228606.4:p.Ser365Thr
ENST00000546567.5:c.388T>A ENSP00000449472.1:p.Ser130Thr
ENST00000547344.5:n.1232T>A
NM_000785.3:c.1093T>A NP_000776.1:p.Ser365Thr
NM_000785.4:c.1093T>A MANE Select NP_000776.1:p.Ser365Thr