Canonical Allele Identifier: CA2619520983

Gene: CYP27B1

Linked Data

• gnomAD v4: 12-57766479-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766479T>C , CM000674.2:g.57766479T>C	GRCh38
NC_000012.11:g.58160262T>C , CM000674.1:g.58160262T>C	GRCh37
NC_000012.10:g.56446529T>C	NCBI36
NG_007076.1:g.5715A>G
NG_047060.1:g.10653A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.108-282A>G
ENST00000713544.1:c.196-282A>G	ENSP00000518840.1:n.196-282A>G
ENST00000713545.1:c.196-282A>G	ENSP00000518841.1:n.196-282A>G
ENST00000228606.9:c.196-282A>G MANE Select	ENSP00000228606.4:n.196-282A>G
ENST00000228606.8:c.196-282A>G	ENSP00000228606.4:n.196-282A>G
ENST00000546609.1:c.108-282A>G
ENST00000547344.5:n.250-282A>G
ENST00000552186.1:n.33A>G
NM_000785.3:c.196-282A>G	NP_000776.1:n.196-282A>G
NM_000785.4:c.196-282A>G MANE Select	NP_000776.1:n.196-282A>G