Canonical Allele Identifier: CA385500867
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58157458A>T (hg19) chr12:g.57763675A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763675A>T , CM000674.2:g.57763675A>T GRCh38
NC_000012.11:g.58157458A>T , CM000674.1:g.58157458A>T GRCh37
NC_000012.10:g.56443725A>T NCBI36
NG_007076.1:g.8519T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1430T>A ENSP00000518840.1:p.Phe477Tyr
ENST00000713545.1:c.*354T>A ENSP00000518841.1:n.*354T>A
ENST00000228606.9:c.1349T>A MANE Select ENSP00000228606.4:p.Phe450Tyr
ENST00000228606.8:c.1349T>A ENSP00000228606.4:p.Phe450Tyr
ENST00000547344.5:n.1488T>A
NM_000785.3:c.1349T>A NP_000776.1:p.Phe450Tyr
NM_000785.4:c.1349T>A MANE Select NP_000776.1:p.Phe450Tyr
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