Canonical Allele Identifier: CA385508032
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766090C>A , CM000674.2:g.57766090C>A GRCh38
NC_000012.11:g.58159873C>A , CM000674.1:g.58159873C>A GRCh37
NC_000012.10:g.56446140C>A NCBI36
NG_007076.1:g.6104G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.215G>T
ENST00000713544.1:c.303G>T ENSP00000518840.1:p.Glu101Asp
ENST00000713545.1:c.303G>T ENSP00000518841.1:p.Glu101Asp
ENST00000228606.9:c.303G>T MANE Select ENSP00000228606.4:p.Glu101Asp
ENST00000228606.8:c.303G>T ENSP00000228606.4:p.Glu101Asp
ENST00000546496.1:n.131G>T
ENST00000546609.1:c.215G>T
ENST00000547344.5:n.357G>T
ENST00000552186.1:n.422G>T
NM_000785.3:c.303G>T NP_000776.1:p.Glu101Asp
NM_000785.4:c.303G>T MANE Select NP_000776.1:p.Glu101Asp