Canonical Allele Identifier: CA2038990929
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766142C= , CM000674.2:g.57766142C= GRCh38
NC_000012.11:g.58159925C= , CM000674.1:g.58159925C= GRCh37
NC_000012.10:g.56446192C= NCBI36
NG_007076.1:g.6052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.163G=
ENST00000713544.1:c.251G= ENSP00000518840.1:p.Arg84=
ENST00000713545.1:c.251G= ENSP00000518841.1:p.Arg84=
ENST00000228606.9:c.251G= MANE Select ENSP00000228606.4:p.Arg84=
ENST00000228606.8:c.251G= ENSP00000228606.4:p.Arg84=
ENST00000546496.1:n.79G=
ENST00000546609.1:c.163G=
ENST00000547344.5:n.305G=
ENST00000552186.1:n.370G=
NM_000785.3:c.251G= NP_000776.1:p.Arg84=
NM_000785.4:c.251G= MANE Select NP_000776.1:p.Arg84=