Canonical Allele Identifier: CA385501082
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58157510A>G (hg19) chr12:g.57763727A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763727A>G , CM000674.2:g.57763727A>G GRCh38
NC_000012.11:g.58157510A>G , CM000674.1:g.58157510A>G GRCh37
NC_000012.10:g.56443777A>G NCBI36
NG_007076.1:g.8467T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1378T>C ENSP00000518840.1:p.Trp460Arg
ENST00000713545.1:c.*302T>C ENSP00000518841.1:n.*302T>C
ENST00000228606.9:c.1297T>C MANE Select ENSP00000228606.4:p.Trp433Arg
ENST00000228606.8:c.1297T>C ENSP00000228606.4:p.Trp433Arg
ENST00000547344.5:n.1436T>C
NM_000785.3:c.1297T>C NP_000776.1:p.Trp433Arg
NM_000785.4:c.1297T>C MANE Select NP_000776.1:p.Trp433Arg
Search 100 bp 5'
Search 100 bp 3'