Canonical Allele Identifier: CA65834632
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1658157
ClinVar RCV Id: RCV002164558
dbSNP Id: rs1045010358
MyVariant Identifiers: chr2:g.219678821G>A (hg19) chr2:g.218814098G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814098G>A , CM000664.2:g.218814098G>A GRCh38
NC_000002.11:g.219678821G>A , CM000664.1:g.219678821G>A GRCh37
NC_000002.10:g.219387065G>A NCBI36
NG_007959.1:g.37350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1095G>A MANE Select ENSP00000258415.4:p.Val365=
ENST00000258415.8:c.1095G>A ENSP00000258415.4:p.Val365=
ENST00000494263.5:n.1529G>A
NM_000784.3:c.1095G>A NP_000775.1:p.Val365=
XM_017003488.2:c.675G>A XP_016858977.1:p.Val225=
NM_000784.4:c.1095G>A MANE Select NP_000775.1:p.Val365=
Search 100 bp 5'
Search 100 bp 3'