Canonical Allele Identifier: CA2619518884
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765932T>C , CM000674.2:g.57765932T>C GRCh38
NC_000012.11:g.58159715T>C , CM000674.1:g.58159715T>C GRCh37
NC_000012.10:g.56445982T>C NCBI36
NG_007076.1:g.6262A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.298+75A>G
ENST00000713544.1:c.386+75A>G ENSP00000518840.1:n.386+75A>G
ENST00000713545.1:c.386+75A>G ENSP00000518841.1:n.386+75A>G
ENST00000228606.9:c.386+75A>G MANE Select ENSP00000228606.4:n.386+75A>G
ENST00000228606.8:c.386+75A>G ENSP00000228606.4:n.386+75A>G
ENST00000546496.1:n.214+75A>G
ENST00000546609.1:c.298+75A>G
ENST00000547344.5:n.440+75A>G
ENST00000552186.1:n.505+75A>G
NM_000785.3:c.386+75A>G NP_000776.1:n.386+75A>G
NM_000785.4:c.386+75A>G MANE Select NP_000776.1:n.386+75A>G