Canonical Allele Identifier: CA385505521
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765175C>T , CM000674.2:g.57765175C>T GRCh38
NC_000012.11:g.58158958C>T , CM000674.1:g.58158958C>T GRCh37
NC_000012.10:g.56445225C>T NCBI36
NG_007076.1:g.7019G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.538G>A
ENST00000713544.1:c.707G>A ENSP00000518840.1:p.Cys236Tyr
ENST00000713545.1:c.684G>A ENSP00000518841.1:p.Leu228=
ENST00000228606.9:c.626G>A MANE Select ENSP00000228606.4:p.Cys209Tyr
ENST00000228606.8:c.626G>A ENSP00000228606.4:p.Cys209Tyr
ENST00000546567.5:c.-80G>A ENSP00000449472.1:n.-80G>A
ENST00000546609.1:c.538G>A
ENST00000547344.5:n.765G>A
ENST00000547451.1:n.426G>A
NM_000785.3:c.626G>A NP_000776.1:p.Cys209Tyr
NM_000785.4:c.626G>A MANE Select NP_000776.1:p.Cys209Tyr