Canonical Allele Identifier: CA385503691
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58158241G>T (hg19) chr12:g.57764458G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764458G>T , CM000674.2:g.57764458G>T GRCh38
NC_000012.11:g.58158241G>T , CM000674.1:g.58158241G>T GRCh37
NC_000012.10:g.56444508G>T NCBI36
NG_007076.1:g.7736C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1137C>A ENSP00000518840.1:p.Ser379Arg
ENST00000713545.1:c.*61C>A ENSP00000518841.1:n.*61C>A
ENST00000228606.9:c.1056C>A MANE Select ENSP00000228606.4:p.Ser352Arg
ENST00000228606.8:c.1056C>A ENSP00000228606.4:p.Ser352Arg
ENST00000546567.5:c.351C>A ENSP00000449472.1:p.Ser117Arg
ENST00000547344.5:n.1195C>A
NM_000785.3:c.1056C>A NP_000776.1:p.Ser352Arg
NM_000785.4:c.1056C>A MANE Select NP_000776.1:p.Ser352Arg
Search 100 bp 5'
Search 100 bp 3'