Canonical Allele Identifier: CA480269630
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58159927C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766144C>A , CM000674.2:g.57766144C>A GRCh38
NC_000012.11:g.58159927C>A , CM000674.1:g.58159927C>A GRCh37
NC_000012.10:g.56446194C>A NCBI36
NG_007076.1:g.6050G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.161G>T
ENST00000713544.1:c.249G>T ENSP00000518840.1:p.Val83=
ENST00000713545.1:c.249G>T ENSP00000518841.1:p.Val83=
ENST00000228606.9:c.249G>T MANE Select ENSP00000228606.4:p.Val83=
ENST00000228606.8:c.249G>T ENSP00000228606.4:p.Val83=
ENST00000546496.1:n.77G>T
ENST00000546609.1:c.161G>T
ENST00000547344.5:n.303G>T
ENST00000552186.1:n.368G>T
NM_000785.3:c.249G>T NP_000776.1:p.Val83=
NM_000785.4:c.249G>T MANE Select NP_000776.1:p.Val83=