Canonical Allele Identifier: CA385503446

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158212G>A (hg19) ; chr12:g.57764429G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764429G>A , CM000674.2:g.57764429G>A	GRCh38
NC_000012.11:g.58158212G>A , CM000674.1:g.58158212G>A	GRCh37
NC_000012.10:g.56444479G>A	NCBI36
NG_007076.1:g.7765C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000713544.1:c.1166C>T	ENSP00000518840.1:p.Thr389Ile
ENST00000713545.1:c.*90C>T	ENSP00000518841.1:n.*90C>T
ENST00000228606.9:c.1085C>T MANE Select	ENSP00000228606.4:p.Thr362Ile
ENST00000228606.8:c.1085C>T	ENSP00000228606.4:p.Thr362Ile
ENST00000546567.5:c.380C>T	ENSP00000449472.1:p.Thr127Ile
ENST00000547344.5:n.1224C>T
NM_000785.3:c.1085C>T	NP_000776.1:p.Thr362Ile
NM_000785.4:c.1085C>T MANE Select	NP_000776.1:p.Thr362Ile