Canonical Allele Identifier: CA431234349
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219679639C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814916C>T , CM000664.2:g.218814916C>T GRCh38
NC_000002.11:g.219679639C>T , CM000664.1:g.219679639C>T GRCh37
NC_000002.10:g.219387883C>T NCBI36
NG_007959.1:g.38168C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1482C>T MANE Select ENSP00000258415.4:p.Ile494=
ENST00000258415.8:c.1482C>T ENSP00000258415.4:p.Ile494=
ENST00000494263.5:n.2194C>T
NM_000784.3:c.1482C>T NP_000775.1:p.Ile494=
XM_017003488.2:c.1062C>T XP_016858977.1:p.Ile354=
NM_000784.4:c.1482C>T MANE Select NP_000775.1:p.Ile494=