Canonical Allele Identifier: CA385500787
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763657A>G , CM000674.2:g.57763657A>G GRCh38
NC_000012.11:g.58157440A>G , CM000674.1:g.58157440A>G GRCh37
NC_000012.10:g.56443707A>G NCBI36
NG_007076.1:g.8537T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1448T>C ENSP00000518840.1:p.Met483Thr
ENST00000713545.1:c.*372T>C ENSP00000518841.1:n.*372T>C
ENST00000228606.9:c.1367T>C MANE Select ENSP00000228606.4:p.Met456Thr
ENST00000228606.8:c.1367T>C ENSP00000228606.4:p.Met456Thr
ENST00000547344.5:n.1506T>C
NM_000785.3:c.1367T>C NP_000776.1:p.Met456Thr
NM_000785.4:c.1367T>C MANE Select NP_000776.1:p.Met456Thr