Canonical Allele Identifier: CA385502664
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58157927A>G (hg19) chr12:g.57764144A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764144A>G , CM000674.2:g.57764144A>G GRCh38
NC_000012.11:g.58157927A>G , CM000674.1:g.58157927A>G GRCh37
NC_000012.10:g.56444194A>G NCBI36
NG_007076.1:g.8050T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1250T>C ENSP00000518840.1:p.Val417Ala
ENST00000713545.1:c.*174T>C ENSP00000518841.1:n.*174T>C
ENST00000228606.9:c.1169T>C MANE Select ENSP00000228606.4:p.Val390Ala
ENST00000228606.8:c.1169T>C ENSP00000228606.4:p.Val390Ala
ENST00000546567.5:c.464T>C ENSP00000449472.1:p.Val155Ala
ENST00000547344.5:n.1308T>C
NM_000785.3:c.1169T>C NP_000776.1:p.Val390Ala
NM_000785.4:c.1169T>C MANE Select NP_000776.1:p.Val390Ala
Search 100 bp 5'
Search 100 bp 3'