Canonical Allele Identifier: CA385505541

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158963C>A (hg19) ; chr12:g.57765180C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765180C>A , CM000674.2:g.57765180C>A	GRCh38
NC_000012.11:g.58158963C>A , CM000674.1:g.58158963C>A	GRCh37
NC_000012.10:g.56445230C>A	NCBI36
NG_007076.1:g.7014G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.533G>T
ENST00000713544.1:c.702G>T	ENSP00000518840.1:p.Leu234Phe
ENST00000713545.1:c.679G>T	ENSP00000518841.1:p.Gly227Trp
ENST00000228606.9:c.621G>T MANE Select	ENSP00000228606.4:p.Leu207Phe
ENST00000228606.8:c.621G>T	ENSP00000228606.4:p.Leu207Phe
ENST00000546567.5:c.-85G>T	ENSP00000449472.1:n.-85G>T
ENST00000546609.1:c.533G>T
ENST00000547344.5:n.760G>T
ENST00000547451.1:n.421G>T
NM_000785.3:c.621G>T	NP_000776.1:p.Leu207Phe
NM_000785.4:c.621G>T MANE Select	NP_000776.1:p.Leu207Phe