Canonical Allele Identifier: CA2039015148
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763677G= , CM000674.2:g.57763677G= GRCh38
NC_000012.11:g.58157460G= , CM000674.1:g.58157460G= GRCh37
NC_000012.10:g.56443727G= NCBI36
NG_007076.1:g.8517C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1428C= ENSP00000518840.1:p.Gly476=
ENST00000713545.1:c.*352C= ENSP00000518841.1:n.*352C=
ENST00000228606.9:c.1347C= MANE Select ENSP00000228606.4:p.Gly449=
ENST00000228606.8:c.1347C= ENSP00000228606.4:p.Gly449=
ENST00000547344.5:n.1486C=
NM_000785.3:c.1347C= NP_000776.1:p.Gly449=
NM_000785.4:c.1347C= MANE Select NP_000776.1:p.Gly449=