Canonical Allele Identifier: CA431234345
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219679636G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814913G>A , CM000664.2:g.218814913G>A GRCh38
NC_000002.11:g.219679636G>A , CM000664.1:g.219679636G>A GRCh37
NC_000002.10:g.219387880G>A NCBI36
NG_007959.1:g.38165G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1479G>A MANE Select ENSP00000258415.4:p.Leu493=
ENST00000258415.8:c.1479G>A ENSP00000258415.4:p.Leu493=
ENST00000494263.5:n.2191G>A
NM_000784.3:c.1479G>A NP_000775.1:p.Leu493=
XM_017003488.2:c.1059G>A XP_016858977.1:p.Leu353=
NM_000784.4:c.1479G>A MANE Select NP_000775.1:p.Leu493=