Canonical Allele Identifier: CA2039015610
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763807G= , CM000674.2:g.57763807G= GRCh38
NC_000012.11:g.58157590G= , CM000674.1:g.58157590G= GRCh37
NC_000012.10:g.56443857G= NCBI36
NG_007076.1:g.8387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1298C= ENSP00000518840.1:p.Thr433=
ENST00000713545.1:c.*222C= ENSP00000518841.1:n.*222C=
ENST00000228606.9:c.1217C= MANE Select ENSP00000228606.4:p.Thr406=
ENST00000228606.8:c.1217C= ENSP00000228606.4:p.Thr406=
ENST00000547344.5:n.1356C=
NM_000785.3:c.1217C= NP_000776.1:p.Thr406=
NM_000785.4:c.1217C= MANE Select NP_000776.1:p.Thr406=