Canonical Allele Identifier: CA385509410
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766156G>T , CM000674.2:g.57766156G>T GRCh38
NC_000012.11:g.58159939G>T , CM000674.1:g.58159939G>T GRCh37
NC_000012.10:g.56446206G>T NCBI36
NG_007076.1:g.6038C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.149C>A
ENST00000713544.1:c.237C>A ENSP00000518840.1:p.Ser79Arg
ENST00000713545.1:c.237C>A ENSP00000518841.1:p.Ser79Arg
ENST00000228606.9:c.237C>A MANE Select ENSP00000228606.4:p.Ser79Arg
ENST00000228606.8:c.237C>A ENSP00000228606.4:p.Ser79Arg
ENST00000546496.1:n.65C>A
ENST00000546609.1:c.149C>A
ENST00000547344.5:n.291C>A
ENST00000552186.1:n.356C>A
NM_000785.3:c.237C>A NP_000776.1:p.Ser79Arg
NM_000785.4:c.237C>A MANE Select NP_000776.1:p.Ser79Arg