Canonical Allele Identifier: CA2039015404
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763754C= , CM000674.2:g.57763754C= GRCh38
NC_000012.11:g.58157537C= , CM000674.1:g.58157537C= GRCh37
NC_000012.10:g.56443804C= NCBI36
NG_007076.1:g.8440G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1351G= ENSP00000518840.1:p.Glu451=
ENST00000713545.1:c.*275G= ENSP00000518841.1:n.*275G=
ENST00000228606.9:c.1270G= MANE Select ENSP00000228606.4:p.Glu424=
ENST00000228606.8:c.1270G= ENSP00000228606.4:p.Glu424=
ENST00000547344.5:n.1409G=
NM_000785.3:c.1270G= NP_000776.1:p.Glu424=
NM_000785.4:c.1270G= MANE Select NP_000776.1:p.Glu424=