Canonical Allele Identifier: CA2697550453
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2734497
ClinVar RCV Id: RCV003504531
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814203G>A , CM000664.2:g.218814203G>A GRCh38
NC_000002.11:g.219678926G>A , CM000664.1:g.219678926G>A GRCh37
NC_000002.10:g.219387170G>A NCBI36
NG_007959.1:g.37455G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.1184+16G>A MANE Select ENSP00000258415.4:n.1184+16G>A
ENST00000258415.8:c.1184+16G>A ENSP00000258415.4:n.1184+16G>A
ENST00000494263.5:n.1634G>A
NM_000784.3:c.1184+16G>A NP_000775.1:n.1184+16G>A
XM_017003488.2:c.764+16G>A XP_016858977.1:n.764+16G>A
NM_000784.4:c.1184+16G>A MANE Select NP_000775.1:n.1184+16G>A
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