Canonical Allele Identifier: CA350586238
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219677317A>G (hg19) chr2:g.218812594A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218812594A>G , CM000664.2:g.218812594A>G GRCh38
NC_000002.11:g.219677317A>G , CM000664.1:g.219677317A>G GRCh37
NC_000002.10:g.219385561A>G NCBI36
NG_007959.1:g.35846A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.689A>G MANE Select ENSP00000258415.4:p.Gln230Arg
ENST00000258415.8:c.689A>G ENSP00000258415.4:p.Gln230Arg
ENST00000411688.1:c.407A>G ENSP00000392671.1:p.Gln136Arg
ENST00000445971.1:c.*150A>G ENSP00000404945.1:n.*150A>G
ENST00000466602.1:n.637A>G
ENST00000494263.5:n.1123A>G
NM_000784.3:c.689A>G NP_000775.1:p.Gln230Arg
XM_017003488.2:c.269A>G XP_016858977.1:p.Gln90Arg
NM_000784.4:c.689A>G MANE Select NP_000775.1:p.Gln230Arg
Search 100 bp 5'
Search 100 bp 3'