Canonical Allele Identifier: CA2112717
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 500768
ClinVar RCV Id: RCV000596057 RCV001429604
dbSNP Id: rs201500822
ExAC: 2:219677418 G / A
gnomAD v2: 2-219677418-G-A
gnomAD v3: 2-218812695-G-A
gnomAD v4: 2-218812695-G-A
MyVariant Identifiers: chr2:g.219677418G>A (hg19) chr2:g.218812695G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812695G>A , CM000664.2:g.218812695G>A GRCh38
NC_000002.11:g.219677418G>A , CM000664.1:g.219677418G>A GRCh37
NC_000002.10:g.219385662G>A NCBI36
NG_007959.1:g.35947G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.790G>A MANE Select ENSP00000258415.4:p.Val264Met
ENST00000258415.8:c.790G>A ENSP00000258415.4:p.Val264Met
ENST00000411688.1:c.508G>A ENSP00000392671.1:p.Val170Met
ENST00000445971.1:c.*251G>A ENSP00000404945.1:n.*251G>A
ENST00000466602.1:n.738G>A
ENST00000494263.5:n.1224G>A
NM_000784.3:c.790G>A NP_000775.1:p.Val264Met
XM_017003488.2:c.370G>A XP_016858977.1:p.Val124Met
NM_000784.4:c.790G>A MANE Select NP_000775.1:p.Val264Met
Search 100 bp 5'
Search 100 bp 3'