Canonical Allele Identifier: CA350591239
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219678754C>A (hg19) chr2:g.218814031C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814031C>A , CM000664.2:g.218814031C>A GRCh38
NC_000002.11:g.219678754C>A , CM000664.1:g.219678754C>A GRCh37
NC_000002.10:g.219386998C>A NCBI36
NG_007959.1:g.37283C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1028C>A MANE Select ENSP00000258415.4:p.Thr343Lys
ENST00000258415.8:c.1028C>A ENSP00000258415.4:p.Thr343Lys
ENST00000445971.1:c.*489C>A ENSP00000404945.1:n.*489C>A
ENST00000466602.1:n.1150C>A
ENST00000494263.5:n.1462C>A
NM_000784.3:c.1028C>A NP_000775.1:p.Thr343Lys
XM_017003488.2:c.608C>A XP_016858977.1:p.Thr203Lys
NM_000784.4:c.1028C>A MANE Select NP_000775.1:p.Thr343Lys
Search 100 bp 5'
Search 100 bp 3'