Canonical Allele Identifier: CA2619518855
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765928del , CM000674.2:g.57765928del GRCh38
NC_000012.11:g.58159711del , CM000674.1:g.58159711del GRCh37
NC_000012.10:g.56445978del NCBI36
NG_007076.1:g.6270del

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.298+83del
ENST00000713544.1:c.386+83del ENSP00000518840.1:n.386+83del
ENST00000713545.1:c.386+83del ENSP00000518841.1:n.386+83del
ENST00000228606.9:c.386+83del MANE Select ENSP00000228606.4:n.386+83del
ENST00000228606.8:c.386+83del ENSP00000228606.4:n.386+83del
ENST00000546496.1:n.214+83del
ENST00000546609.1:c.298+83del
ENST00000547344.5:n.440+83del
ENST00000552186.1:n.505+83del
NM_000785.3:c.386+83del NP_000776.1:n.386+83del
NM_000785.4:c.386+83del MANE Select NP_000776.1:n.386+83del