Canonical Allele Identifier: CA6658468

Gene: CYP27B1

Linked Data

• dbSNP Id: rs368234045
• ExAC: 12:58159414 C / A
• gnomAD v2: 12-58159414-C-A
• gnomAD v3: 12-57765631-C-A
• gnomAD v4: 12-57765631-C-A
• MyVariant Identifiers: chr12:g.58159414C>A (hg19) ; chr12:g.57765631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765631C>A , CM000674.2:g.57765631C>A	GRCh38
NC_000012.11:g.58159414C>A , CM000674.1:g.58159414C>A	GRCh37
NC_000012.10:g.56445681C>A	NCBI36
NG_007076.1:g.6563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-132G>T
ENST00000713544.1:c.387-51G>T	ENSP00000518840.1:n.387-51G>T
ENST00000713545.1:c.387-74G>T	ENSP00000518841.1:n.387-74G>T
ENST00000228606.9:c.387-132G>T MANE Select	ENSP00000228606.4:n.387-132G>T
ENST00000228606.8:c.387-132G>T	ENSP00000228606.4:n.387-132G>T
ENST00000546496.1:n.215-132G>T
ENST00000546567.5:c.-451G>T	ENSP00000449472.1:n.-451G>T
ENST00000546609.1:c.299-132G>T
ENST00000547344.5:n.441-132G>T
ENST00000547451.1:n.55G>T
ENST00000552186.1:n.506-132G>T
NM_000785.3:c.387-132G>T	NP_000776.1:n.387-132G>T
NM_000785.4:c.387-132G>T MANE Select	NP_000776.1:n.387-132G>T