Canonical Allele Identifier: CA764918453
Gene: CYP27A1 HGNC NCBI

Linked Data

dbSNP Id: rs1366431065
MyVariant Identifiers: chr2:g.219678927T>C (hg19) chr2:g.218814204T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218814204T>C , CM000664.2:g.218814204T>C GRCh38
NC_000002.11:g.219678927T>C , CM000664.1:g.219678927T>C GRCh37
NC_000002.10:g.219387171T>C NCBI36
NG_007959.1:g.37456T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.1184+17T>C MANE Select ENSP00000258415.4:n.1184+17T>C
ENST00000258415.8:c.1184+17T>C ENSP00000258415.4:n.1184+17T>C
ENST00000494263.5:n.1635T>C
NM_000784.3:c.1184+17T>C NP_000775.1:n.1184+17T>C
XM_017003488.2:c.764+17T>C XP_016858977.1:n.764+17T>C
NM_000784.4:c.1184+17T>C MANE Select NP_000775.1:n.1184+17T>C
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