Canonical Allele Identifier: CA480401664
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2820339
ClinVar RCV Id: RCV003709138
MyVariant Identifiers: chr12:g.58158220G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764437G>A , CM000674.2:g.57764437G>A GRCh38
NC_000012.11:g.58158220G>A , CM000674.1:g.58158220G>A GRCh37
NC_000012.10:g.56444487G>A NCBI36
NG_007076.1:g.7757C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1158C>T ENSP00000518840.1:p.Pro386=
ENST00000713545.1:c.*82C>T ENSP00000518841.1:n.*82C>T
ENST00000228606.9:c.1077C>T MANE Select ENSP00000228606.4:p.Pro359=
ENST00000228606.8:c.1077C>T ENSP00000228606.4:p.Pro359=
ENST00000546567.5:c.372C>T ENSP00000449472.1:p.Pro124=
ENST00000547344.5:n.1216C>T
NM_000785.3:c.1077C>T NP_000776.1:p.Pro359=
NM_000785.4:c.1077C>T MANE Select NP_000776.1:p.Pro359=