Canonical Allele Identifier: CA605325322

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1269895331
• gnomAD v2: 12-58159450-T-C
• gnomAD v4: 12-57765667-T-C
• MyVariant Identifiers: chr12:g.58159450T>C (hg19) ; chr12:g.57765667T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765667T>C , CM000674.2:g.57765667T>C	GRCh38
NC_000012.11:g.58159450T>C , CM000674.1:g.58159450T>C	GRCh37
NC_000012.10:g.56445717T>C	NCBI36
NG_007076.1:g.6527A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-168A>G
ENST00000713544.1:c.387-87A>G	ENSP00000518840.1:n.387-87A>G
ENST00000713545.1:c.387-110A>G	ENSP00000518841.1:n.387-110A>G
ENST00000228606.9:c.387-168A>G MANE Select	ENSP00000228606.4:n.387-168A>G
ENST00000228606.8:c.387-168A>G	ENSP00000228606.4:n.387-168A>G
ENST00000546496.1:n.215-168A>G
ENST00000546567.5:c.-487A>G	ENSP00000449472.1:n.-487A>G
ENST00000546609.1:c.299-168A>G
ENST00000547344.5:n.441-168A>G
ENST00000547451.1:n.19A>G
ENST00000552186.1:n.506-168A>G
NM_000785.3:c.387-168A>G	NP_000776.1:n.387-168A>G
NM_000785.4:c.387-168A>G MANE Select	NP_000776.1:n.387-168A>G