Canonical Allele Identifier: CA480401635
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58158208A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764425A>C , CM000674.2:g.57764425A>C GRCh38
NC_000012.11:g.58158208A>C , CM000674.1:g.58158208A>C GRCh37
NC_000012.10:g.56444475A>C NCBI36
NG_007076.1:g.7769T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1170T>G ENSP00000518840.1:p.Val390=
ENST00000713545.1:c.*94T>G ENSP00000518841.1:n.*94T>G
ENST00000228606.9:c.1089T>G MANE Select ENSP00000228606.4:p.Val363=
ENST00000228606.8:c.1089T>G ENSP00000228606.4:p.Val363=
ENST00000546567.5:c.384T>G ENSP00000449472.1:p.Val128=
ENST00000547344.5:n.1228T>G
NM_000785.3:c.1089T>G NP_000776.1:p.Val363=
NM_000785.4:c.1089T>G MANE Select NP_000776.1:p.Val363=