Canonical Allele Identifier: CA480403141

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1312398461
• gnomAD v4: 12-57765147-C-G
• MyVariant Identifiers: chr12:g.58158930C>G (hg19) ; chr12:g.57765147C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765147C>G , CM000674.2:g.57765147C>G	GRCh38
NC_000012.11:g.58158930C>G , CM000674.1:g.58158930C>G	GRCh37
NC_000012.10:g.56445197C>G	NCBI36
NG_007076.1:g.7047G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000546609.2:n.566G>C
ENST00000713544.1:c.735G>C	ENSP00000518840.1:p.Thr245=
ENST00000713545.1:c.712G>C	ENSP00000518841.1:p.Gly238Arg
ENST00000228606.9:c.654G>C MANE Select	ENSP00000228606.4:p.Thr218=
ENST00000228606.8:c.654G>C	ENSP00000228606.4:p.Thr218=
ENST00000546567.5:c.-52G>C	ENSP00000449472.1:n.-52G>C
ENST00000546609.1:c.566G>C
ENST00000547344.5:n.793G>C
ENST00000547451.1:n.454G>C
NM_000785.3:c.654G>C	NP_000776.1:p.Thr218=
NM_000785.4:c.654G>C MANE Select	NP_000776.1:p.Thr218=