Canonical Allele Identifier: CA385502307
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764102T>G , CM000674.2:g.57764102T>G GRCh38
NC_000012.11:g.58157885T>G , CM000674.1:g.58157885T>G GRCh37
NC_000012.10:g.56444152T>G NCBI36
NG_007076.1:g.8092A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1292A>C ENSP00000518840.1:p.Lys431Thr
ENST00000713545.1:c.*216A>C ENSP00000518841.1:n.*216A>C
ENST00000228606.9:c.1211A>C MANE Select ENSP00000228606.4:p.Lys404Thr
ENST00000228606.8:c.1211A>C ENSP00000228606.4:p.Lys404Thr
ENST00000547344.5:n.1350A>C
NM_000785.3:c.1211A>C NP_000776.1:p.Lys404Thr
NM_000785.4:c.1211A>C MANE Select NP_000776.1:p.Lys404Thr