Canonical Allele Identifier: CA237815339

Gene: CYP27B1

Linked Data

• dbSNP Id: rs925569440
• gnomAD v2: 12-58159444-C-T
• gnomAD v3: 12-57765661-C-T
• gnomAD v4: 12-57765661-C-T
• MyVariant Identifiers: chr12:g.58159444C>T (hg19) ; chr12:g.57765661C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765661C>T , CM000674.2:g.57765661C>T	GRCh38
NC_000012.11:g.58159444C>T , CM000674.1:g.58159444C>T	GRCh37
NC_000012.10:g.56445711C>T	NCBI36
NG_007076.1:g.6533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-162G>A
ENST00000713544.1:c.387-81G>A	ENSP00000518840.1:n.387-81G>A
ENST00000713545.1:c.387-104G>A	ENSP00000518841.1:n.387-104G>A
ENST00000228606.9:c.387-162G>A MANE Select	ENSP00000228606.4:n.387-162G>A
ENST00000228606.8:c.387-162G>A	ENSP00000228606.4:n.387-162G>A
ENST00000546496.1:n.215-162G>A
ENST00000546567.5:c.-481G>A	ENSP00000449472.1:n.-481G>A
ENST00000546609.1:c.299-162G>A
ENST00000547344.5:n.441-162G>A
ENST00000547451.1:n.25G>A
ENST00000552186.1:n.506-162G>A
NM_000785.3:c.387-162G>A	NP_000776.1:n.387-162G>A
NM_000785.4:c.387-162G>A MANE Select	NP_000776.1:n.387-162G>A