Canonical Allele Identifier: CA2726347200

Gene: CYP27B1

Linked Data

• dbSNP Id: rs2140397361

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765636C>G , CM000674.2:g.57765636C>G	GRCh38
NC_000012.11:g.58159419C>G , CM000674.1:g.58159419C>G	GRCh37
NC_000012.10:g.56445686C>G	NCBI36
NG_007076.1:g.6558G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.299-137G>C
ENST00000713544.1:c.387-56G>C	ENSP00000518840.1:n.387-56G>C
ENST00000713545.1:c.387-79G>C	ENSP00000518841.1:n.387-79G>C
ENST00000228606.9:c.387-137G>C MANE Select	ENSP00000228606.4:n.387-137G>C
ENST00000228606.8:c.387-137G>C	ENSP00000228606.4:n.387-137G>C
ENST00000546496.1:n.215-137G>C
ENST00000546567.5:c.-456G>C	ENSP00000449472.1:n.-456G>C
ENST00000546609.1:c.299-137G>C
ENST00000547344.5:n.441-137G>C
ENST00000547451.1:n.50G>C
ENST00000552186.1:n.506-137G>C
NM_000785.3:c.387-137G>C	NP_000776.1:n.387-137G>C
NM_000785.4:c.387-137G>C MANE Select	NP_000776.1:n.387-137G>C