Canonical Allele Identifier: CA385502383
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001177
ClinVar RCV Id: RCV001297431
dbSNP Id: rs1955339362

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764115A>C , CM000674.2:g.57764115A>C GRCh38
NC_000012.11:g.58157898A>C , CM000674.1:g.58157898A>C GRCh37
NC_000012.10:g.56444165A>C NCBI36
NG_007076.1:g.8079T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1279T>G ENSP00000518840.1:p.Tyr427Asp
ENST00000713545.1:c.*203T>G ENSP00000518841.1:n.*203T>G
ENST00000228606.9:c.1198T>G MANE Select ENSP00000228606.4:p.Tyr400Asp
ENST00000228606.8:c.1198T>G ENSP00000228606.4:p.Tyr400Asp
ENST00000547344.5:n.1337T>G
NM_000785.3:c.1198T>G NP_000776.1:p.Tyr400Asp
NM_000785.4:c.1198T>G MANE Select NP_000776.1:p.Tyr400Asp