Canonical Allele Identifier: CA6658249
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 749236
ClinVar RCV Id: RCV000926092
dbSNP Id: rs764387303

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764527A>G , CM000674.2:g.57764527A>G GRCh38
NC_000012.11:g.58158310A>G , CM000674.1:g.58158310A>G GRCh37
NC_000012.10:g.56444577A>G NCBI36
NG_007076.1:g.7667T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1068T>C ENSP00000518840.1:p.Ala356=
ENST00000713545.1:c.1045T>C ENSP00000518841.1:p.Ser349Pro
ENST00000228606.9:c.987T>C MANE Select ENSP00000228606.4:p.Ala329=
ENST00000228606.8:c.987T>C ENSP00000228606.4:p.Ala329=
ENST00000546567.5:c.282T>C ENSP00000449472.1:p.Ala94=
ENST00000547344.5:n.1126T>C
NM_000785.3:c.987T>C NP_000776.1:p.Ala329=
NM_000785.4:c.987T>C MANE Select NP_000776.1:p.Ala329=