Canonical Allele Identifier: CA385502748
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764154T>C , CM000674.2:g.57764154T>C GRCh38
NC_000012.11:g.58157937T>C , CM000674.1:g.58157937T>C GRCh37
NC_000012.10:g.56444204T>C NCBI36
NG_007076.1:g.8040A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1240A>G ENSP00000518840.1:p.Asn414Asp
ENST00000713545.1:c.*164A>G ENSP00000518841.1:n.*164A>G
ENST00000228606.9:c.1159A>G MANE Select ENSP00000228606.4:p.Asn387Asp
ENST00000228606.8:c.1159A>G ENSP00000228606.4:p.Asn387Asp
ENST00000546567.5:c.454A>G ENSP00000449472.1:p.Asn152Asp
ENST00000547344.5:n.1298A>G
NM_000785.3:c.1159A>G NP_000776.1:p.Asn387Asp
NM_000785.4:c.1159A>G MANE Select NP_000776.1:p.Asn387Asp