Canonical Allele Identifier: CA6658225
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2185800
ClinVar RCV Id: RCV002596330
dbSNP Id: rs373672754

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764428A>T , CM000674.2:g.57764428A>T GRCh38
NC_000012.11:g.58158211A>T , CM000674.1:g.58158211A>T GRCh37
NC_000012.10:g.56444478A>T NCBI36
NG_007076.1:g.7766T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1167T>A ENSP00000518840.1:p.Thr389=
ENST00000713545.1:c.*91T>A ENSP00000518841.1:n.*91T>A
ENST00000228606.9:c.1086T>A MANE Select ENSP00000228606.4:p.Thr362=
ENST00000228606.8:c.1086T>A ENSP00000228606.4:p.Thr362=
ENST00000546567.5:c.381T>A ENSP00000449472.1:p.Thr127=
ENST00000547344.5:n.1225T>A
NM_000785.3:c.1086T>A NP_000776.1:p.Thr362=
NM_000785.4:c.1086T>A MANE Select NP_000776.1:p.Thr362=