Canonical Allele Identifier: CA2038990635
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766020C= , CM000674.2:g.57766020C= GRCh38
NC_000012.11:g.58159803C= , CM000674.1:g.58159803C= GRCh37
NC_000012.10:g.56446070C= NCBI36
NG_007076.1:g.6174G=

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.285G=
ENST00000713544.1:c.373G= ENSP00000518840.1:p.Gly125=
ENST00000713545.1:c.373G= ENSP00000518841.1:p.Gly125=
ENST00000228606.9:c.373G= MANE Select ENSP00000228606.4:p.Gly125=
ENST00000228606.8:c.373G= ENSP00000228606.4:p.Gly125=
ENST00000546496.1:n.201G=
ENST00000546609.1:c.285G=
ENST00000547344.5:n.427G=
ENST00000552186.1:n.492G=
NM_000785.3:c.373G= NP_000776.1:p.Gly125=
NM_000785.4:c.373G= MANE Select NP_000776.1:p.Gly125=