Canonical Allele Identifier: CA2039016142
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764103T= , CM000674.2:g.57764103T= GRCh38
NC_000012.11:g.58157886T= , CM000674.1:g.58157886T= GRCh37
NC_000012.10:g.56444153T= NCBI36
NG_007076.1:g.8091A=

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1291A= ENSP00000518840.1:p.Lys431=
ENST00000713545.1:c.*215A= ENSP00000518841.1:n.*215A=
ENST00000228606.9:c.1210A= MANE Select ENSP00000228606.4:p.Lys404=
ENST00000228606.8:c.1210A= ENSP00000228606.4:p.Lys404=
ENST00000547344.5:n.1349A=
NM_000785.3:c.1210A= NP_000776.1:p.Lys404=
NM_000785.4:c.1210A= MANE Select NP_000776.1:p.Lys404=