Canonical Allele Identifier: CA431234220
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219678878G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814155G>C , CM000664.2:g.218814155G>C GRCh38
NC_000002.11:g.219678878G>C , CM000664.1:g.219678878G>C GRCh37
NC_000002.10:g.219387122G>C NCBI36
NG_007959.1:g.37407G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.1152G>C MANE Select ENSP00000258415.4:p.Pro384=
ENST00000258415.8:c.1152G>C ENSP00000258415.4:p.Pro384=
ENST00000494263.5:n.1586G>C
NM_000784.3:c.1152G>C NP_000775.1:p.Pro384=
XM_017003488.2:c.732G>C XP_016858977.1:p.Pro244=
NM_000784.4:c.1152G>C MANE Select NP_000775.1:p.Pro384=
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