Canonical Allele Identifier: CA6658485
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs774677094

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766023A>C , CM000674.2:g.57766023A>C GRCh38
NC_000012.11:g.58159806A>C , CM000674.1:g.58159806A>C GRCh37
NC_000012.10:g.56446073A>C NCBI36
NG_007076.1:g.6171T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.282T>G
ENST00000713544.1:c.370T>G ENSP00000518840.1:p.Cys124Gly
ENST00000713545.1:c.370T>G ENSP00000518841.1:p.Cys124Gly
ENST00000228606.9:c.370T>G MANE Select ENSP00000228606.4:p.Cys124Gly
ENST00000228606.8:c.370T>G ENSP00000228606.4:p.Cys124Gly
ENST00000546496.1:n.198T>G
ENST00000546609.1:c.282T>G
ENST00000547344.5:n.424T>G
ENST00000552186.1:n.489T>G
NM_000785.3:c.370T>G NP_000776.1:p.Cys124Gly
NM_000785.4:c.370T>G MANE Select NP_000776.1:p.Cys124Gly