Canonical Allele Identifier: CA385509336
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766140T>C , CM000674.2:g.57766140T>C GRCh38
NC_000012.11:g.58159923T>C , CM000674.1:g.58159923T>C GRCh37
NC_000012.10:g.56446190T>C NCBI36
NG_007076.1:g.6054A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.165A>G
ENST00000713544.1:c.253A>G ENSP00000518840.1:p.Thr85Ala
ENST00000713545.1:c.253A>G ENSP00000518841.1:p.Thr85Ala
ENST00000228606.9:c.253A>G MANE Select ENSP00000228606.4:p.Thr85Ala
ENST00000228606.8:c.253A>G ENSP00000228606.4:p.Thr85Ala
ENST00000546496.1:n.81A>G
ENST00000546609.1:c.165A>G
ENST00000547344.5:n.307A>G
ENST00000552186.1:n.372A>G
NM_000785.3:c.253A>G NP_000776.1:p.Thr85Ala
NM_000785.4:c.253A>G MANE Select NP_000776.1:p.Thr85Ala