Canonical Allele Identifier: CA385507680
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766035G>C , CM000674.2:g.57766035G>C GRCh38
NC_000012.11:g.58159818G>C , CM000674.1:g.58159818G>C GRCh37
NC_000012.10:g.56446085G>C NCBI36
NG_007076.1:g.6159C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.270C>G
ENST00000713544.1:c.358C>G ENSP00000518840.1:p.Arg120Gly
ENST00000713545.1:c.358C>G ENSP00000518841.1:p.Arg120Gly
ENST00000228606.9:c.358C>G MANE Select ENSP00000228606.4:p.Arg120Gly
ENST00000228606.8:c.358C>G ENSP00000228606.4:p.Arg120Gly
ENST00000546496.1:n.186C>G
ENST00000546609.1:c.270C>G
ENST00000547344.5:n.412C>G
ENST00000552186.1:n.477C>G
NM_000785.3:c.358C>G NP_000776.1:p.Arg120Gly
NM_000785.4:c.358C>G MANE Select NP_000776.1:p.Arg120Gly