Canonical Allele Identifier: CA385505539
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765180C>G , CM000674.2:g.57765180C>G GRCh38
NC_000012.11:g.58158963C>G , CM000674.1:g.58158963C>G GRCh37
NC_000012.10:g.56445230C>G NCBI36
NG_007076.1:g.7014G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.533G>C
ENST00000713544.1:c.702G>C ENSP00000518840.1:p.Leu234Phe
ENST00000713545.1:c.679G>C ENSP00000518841.1:p.Gly227Arg
ENST00000228606.9:c.621G>C MANE Select ENSP00000228606.4:p.Leu207Phe
ENST00000228606.8:c.621G>C ENSP00000228606.4:p.Leu207Phe
ENST00000546567.5:c.-85G>C ENSP00000449472.1:n.-85G>C
ENST00000546609.1:c.533G>C
ENST00000547344.5:n.760G>C
ENST00000547451.1:n.421G>C
NM_000785.3:c.621G>C NP_000776.1:p.Leu207Phe
NM_000785.4:c.621G>C MANE Select NP_000776.1:p.Leu207Phe