Canonical Allele Identifier: CA350576333
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219647073C>A (hg19) chr2:g.218782350C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218782350C>A , CM000664.2:g.218782350C>A GRCh38
NC_000002.11:g.219647073C>A , CM000664.1:g.219647073C>A GRCh37
NC_000002.10:g.219355317C>A NCBI36
NG_007959.1:g.5602C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.168C>A MANE Select ENSP00000258415.4:p.Ser56Arg
ENST00000258415.8:c.168C>A ENSP00000258415.4:p.Ser56Arg
ENST00000445971.1:c.168C>A ENSP00000404945.1:p.Ser56Arg
ENST00000466602.1:n.177C>A
ENST00000494263.5:n.602C>A
NM_000784.3:c.168C>A NP_000775.1:p.Ser56Arg
XM_017003488.2:c.-62C>A XP_016858977.1:n.-62C>A
NM_000784.4:c.168C>A MANE Select NP_000775.1:p.Ser56Arg
Search 100 bp 5'
Search 100 bp 3'