Canonical Allele Identifier: CA385500768
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763652T>C , CM000674.2:g.57763652T>C GRCh38
NC_000012.11:g.58157435T>C , CM000674.1:g.58157435T>C GRCh37
NC_000012.10:g.56443702T>C NCBI36
NG_007076.1:g.8542A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1453A>G ENSP00000518840.1:p.Arg485Gly
ENST00000713545.1:c.*377A>G ENSP00000518841.1:n.*377A>G
ENST00000228606.9:c.1372A>G MANE Select ENSP00000228606.4:p.Arg458Gly
ENST00000228606.8:c.1372A>G ENSP00000228606.4:p.Arg458Gly
ENST00000547344.5:n.1511A>G
NM_000785.3:c.1372A>G NP_000776.1:p.Arg458Gly
NM_000785.4:c.1372A>G MANE Select NP_000776.1:p.Arg458Gly