Canonical Allele Identifier: CA385502752
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58157937T>G (hg19) chr12:g.57764154T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764154T>G , CM000674.2:g.57764154T>G GRCh38
NC_000012.11:g.58157937T>G , CM000674.1:g.58157937T>G GRCh37
NC_000012.10:g.56444204T>G NCBI36
NG_007076.1:g.8040A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1240A>C ENSP00000518840.1:p.Asn414His
ENST00000713545.1:c.*164A>C ENSP00000518841.1:n.*164A>C
ENST00000228606.9:c.1159A>C MANE Select ENSP00000228606.4:p.Asn387His
ENST00000228606.8:c.1159A>C ENSP00000228606.4:p.Asn387His
ENST00000546567.5:c.454A>C ENSP00000449472.1:p.Asn152His
ENST00000547344.5:n.1298A>C
NM_000785.3:c.1159A>C NP_000776.1:p.Asn387His
NM_000785.4:c.1159A>C MANE Select NP_000776.1:p.Asn387His
Search 100 bp 5'
Search 100 bp 3'