Canonical Allele Identifier: CA2038990020
Gene: CYP27B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765658C= , CM000674.2:g.57765658C= GRCh38
NC_000012.11:g.58159441C= , CM000674.1:g.58159441C= GRCh37
NC_000012.10:g.56445708C= NCBI36
NG_007076.1:g.6536G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.299-159G=
ENST00000713544.1:c.387-78G= ENSP00000518840.1:n.387-78G=
ENST00000713545.1:c.387-101G= ENSP00000518841.1:n.387-101G=
ENST00000228606.9:c.387-159G= MANE Select ENSP00000228606.4:n.387-159G=
ENST00000228606.8:c.387-159G= ENSP00000228606.4:n.387-159G=
ENST00000546496.1:n.215-159G=
ENST00000546567.5:c.-478G= ENSP00000449472.1:n.-478G=
ENST00000546609.1:c.299-159G=
ENST00000547344.5:n.441-159G=
ENST00000547451.1:n.28G=
ENST00000552186.1:n.506-159G=
NM_000785.3:c.387-159G= NP_000776.1:n.387-159G=
NM_000785.4:c.387-159G= MANE Select NP_000776.1:n.387-159G=
Search 100 bp 5'
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