Canonical Allele Identifier: CA431234344
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219679634C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814911C>T , CM000664.2:g.218814911C>T GRCh38
NC_000002.11:g.219679634C>T , CM000664.1:g.219679634C>T GRCh37
NC_000002.10:g.219387878C>T NCBI36
NG_007959.1:g.38163C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1477C>T MANE Select ENSP00000258415.4:p.Leu493=
ENST00000258415.8:c.1477C>T ENSP00000258415.4:p.Leu493=
ENST00000494263.5:n.2189C>T
NM_000784.3:c.1477C>T NP_000775.1:p.Leu493=
XM_017003488.2:c.1057C>T XP_016858977.1:p.Leu353=
NM_000784.4:c.1477C>T MANE Select NP_000775.1:p.Leu493=