Canonical Allele Identifier: CA2039015892
Gene: CYP27B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763981C= , CM000674.2:g.57763981C= GRCh38
NC_000012.11:g.58157764C= , CM000674.1:g.58157764C= GRCh37
NC_000012.10:g.56444031C= NCBI36
NG_007076.1:g.8213G=

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1296+117G= ENSP00000518840.1:n.1296+117G=
ENST00000713545.1:c.*220+117G= ENSP00000518841.1:n.*220+117G=
ENST00000228606.9:c.1215+117G= MANE Select ENSP00000228606.4:n.1215+117G=
ENST00000228606.8:c.1215+117G= ENSP00000228606.4:n.1215+117G=
ENST00000547344.5:n.1354+117G=
NM_000785.3:c.1215+117G= NP_000776.1:n.1215+117G=
NM_000785.4:c.1215+117G= MANE Select NP_000776.1:n.1215+117G=
Search 100 bp 5'
Search 100 bp 3'