Canonical Allele Identifier: CA2039015384
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763748T= , CM000674.2:g.57763748T= GRCh38
NC_000012.11:g.58157531T= , CM000674.1:g.58157531T= GRCh37
NC_000012.10:g.56443798T= NCBI36
NG_007076.1:g.8446A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1357A= ENSP00000518840.1:p.Asn453=
ENST00000713545.1:c.*281A= ENSP00000518841.1:n.*281A=
ENST00000228606.9:c.1276A= MANE Select ENSP00000228606.4:p.Asn426=
ENST00000228606.8:c.1276A= ENSP00000228606.4:p.Asn426=
ENST00000547344.5:n.1415A=
NM_000785.3:c.1276A= NP_000776.1:p.Asn426=
NM_000785.4:c.1276A= MANE Select NP_000776.1:p.Asn426=