Canonical Allele Identifier: CA385503418
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764421A>C , CM000674.2:g.57764421A>C GRCh38
NC_000012.11:g.58158204A>C , CM000674.1:g.58158204A>C GRCh37
NC_000012.10:g.56444471A>C NCBI36
NG_007076.1:g.7773T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1174T>G ENSP00000518840.1:p.Ser392Ala
ENST00000713545.1:c.*98T>G ENSP00000518841.1:n.*98T>G
ENST00000228606.9:c.1093T>G MANE Select ENSP00000228606.4:p.Ser365Ala
ENST00000228606.8:c.1093T>G ENSP00000228606.4:p.Ser365Ala
ENST00000546567.5:c.388T>G ENSP00000449472.1:p.Ser130Ala
ENST00000547344.5:n.1232T>G
NM_000785.3:c.1093T>G NP_000776.1:p.Ser365Ala
NM_000785.4:c.1093T>G MANE Select NP_000776.1:p.Ser365Ala