Canonical Allele Identifier: CA2038990434
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765922T= , CM000674.2:g.57765922T= GRCh38
NC_000012.11:g.58159705T= , CM000674.1:g.58159705T= GRCh37
NC_000012.10:g.56445972T= NCBI36
NG_007076.1:g.6272A=

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.298+85A=
ENST00000713544.1:c.386+85A= ENSP00000518840.1:n.386+85A=
ENST00000713545.1:c.386+85A= ENSP00000518841.1:n.386+85A=
ENST00000228606.9:c.386+85A= MANE Select ENSP00000228606.4:n.386+85A=
ENST00000228606.8:c.386+85A= ENSP00000228606.4:n.386+85A=
ENST00000546496.1:n.214+85A=
ENST00000546609.1:c.298+85A=
ENST00000547344.5:n.440+85A=
ENST00000552186.1:n.505+85A=
NM_000785.3:c.386+85A= NP_000776.1:n.386+85A=
NM_000785.4:c.386+85A= MANE Select NP_000776.1:n.386+85A=