Canonical Allele Identifier: CA385505145
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765023T>C , CM000674.2:g.57765023T>C GRCh38
NC_000012.11:g.58158806T>C , CM000674.1:g.58158806T>C GRCh37
NC_000012.10:g.56445073T>C NCBI36
NG_007076.1:g.7171A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.690A>G
ENST00000713544.1:c.859A>G ENSP00000518840.1:p.Met287Val
ENST00000713545.1:c.836A>G ENSP00000518841.1:p.Asp279Gly
ENST00000228606.9:c.778A>G MANE Select ENSP00000228606.4:p.Met260Val
ENST00000228606.8:c.778A>G ENSP00000228606.4:p.Met260Val
ENST00000546567.5:c.73A>G ENSP00000449472.1:p.Met25Val
ENST00000546609.1:c.690A>G
ENST00000547344.5:n.917A>G
ENST00000547451.1:n.578A>G
NM_000785.3:c.778A>G NP_000776.1:p.Met260Val
NM_000785.4:c.778A>G MANE Select NP_000776.1:p.Met260Val