Canonical Allele Identifier: CA431234145
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219678779C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814056C>A , CM000664.2:g.218814056C>A GRCh38
NC_000002.11:g.219678779C>A , CM000664.1:g.219678779C>A GRCh37
NC_000002.10:g.219387023C>A NCBI36
NG_007959.1:g.37308C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1053C>A MANE Select ENSP00000258415.4:p.Leu351=
ENST00000258415.8:c.1053C>A ENSP00000258415.4:p.Leu351=
ENST00000445971.1:c.*514C>A ENSP00000404945.1:n.*514C>A
ENST00000466602.1:n.1175C>A
ENST00000494263.5:n.1487C>A
NM_000784.3:c.1053C>A NP_000775.1:p.Leu351=
XM_017003488.2:c.633C>A XP_016858977.1:p.Leu211=
NM_000784.4:c.1053C>A MANE Select NP_000775.1:p.Leu351=
Search 100 bp 5'
Search 100 bp 3'