Canonical Allele Identifier: CA385505117
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765012A>C , CM000674.2:g.57765012A>C GRCh38
NC_000012.11:g.58158795A>C , CM000674.1:g.58158795A>C GRCh37
NC_000012.10:g.56445062A>C NCBI36
NG_007076.1:g.7182T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.701T>G
ENST00000713544.1:c.870T>G ENSP00000518840.1:p.Phe290Leu
ENST00000713545.1:c.847T>G ENSP00000518841.1:p.Cys283Gly
ENST00000228606.9:c.789T>G MANE Select ENSP00000228606.4:p.Phe263Leu
ENST00000228606.8:c.789T>G ENSP00000228606.4:p.Phe263Leu
ENST00000546567.5:c.84T>G ENSP00000449472.1:p.Phe28Leu
ENST00000546609.1:c.701T>G
ENST00000547344.5:n.928T>G
ENST00000547451.1:n.589T>G
NM_000785.3:c.789T>G NP_000776.1:p.Phe263Leu
NM_000785.4:c.789T>G MANE Select NP_000776.1:p.Phe263Leu