Canonical Allele Identifier: CA2038988815
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765128C= , CM000674.2:g.57765128C= GRCh38
NC_000012.11:g.58158911C= , CM000674.1:g.58158911C= GRCh37
NC_000012.10:g.56445178C= NCBI36
NG_007076.1:g.7066G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.585G=
ENST00000713544.1:c.754G= ENSP00000518840.1:p.Val252=
ENST00000713545.1:c.731G= ENSP00000518841.1:p.Cys244=
ENST00000228606.9:c.673G= MANE Select ENSP00000228606.4:p.Val225=
ENST00000228606.8:c.673G= ENSP00000228606.4:p.Val225=
ENST00000546567.5:c.-33G= ENSP00000449472.1:n.-33G=
ENST00000546609.1:c.585G=
ENST00000547344.5:n.812G=
ENST00000547451.1:n.473G=
NM_000785.3:c.673G= NP_000776.1:p.Val225=
NM_000785.4:c.673G= MANE Select NP_000776.1:p.Val225=