Canonical Allele Identifier: CA385505142

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158805A>G (hg19) ; chr12:g.57765022A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765022A>G , CM000674.2:g.57765022A>G	GRCh38
NC_000012.11:g.58158805A>G , CM000674.1:g.58158805A>G	GRCh37
NC_000012.10:g.56445072A>G	NCBI36
NG_007076.1:g.7172T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.691T>C
ENST00000713544.1:c.860T>C	ENSP00000518840.1:p.Met287Thr
ENST00000713545.1:c.837T>C	ENSP00000518841.1:p.Asp279=
ENST00000228606.9:c.779T>C MANE Select	ENSP00000228606.4:p.Met260Thr
ENST00000228606.8:c.779T>C	ENSP00000228606.4:p.Met260Thr
ENST00000546567.5:c.74T>C	ENSP00000449472.1:p.Met25Thr
ENST00000546609.1:c.691T>C
ENST00000547344.5:n.918T>C
ENST00000547451.1:n.579T>C
NM_000785.3:c.779T>C	NP_000776.1:p.Met260Thr
NM_000785.4:c.779T>C MANE Select	NP_000776.1:p.Met260Thr