Canonical Allele Identifier: CA350576884
Gene: CYP27A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219647131G>T (hg19) chr2:g.218782408G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218782408G>T , CM000664.2:g.218782408G>T GRCh38
NC_000002.11:g.219647131G>T , CM000664.1:g.219647131G>T GRCh37
NC_000002.10:g.219355375G>T NCBI36
NG_007959.1:g.5660G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258415.9:c.226G>T MANE Select ENSP00000258415.4:p.Gly76Cys
ENST00000258415.8:c.226G>T ENSP00000258415.4:p.Gly76Cys
ENST00000445971.1:c.226G>T ENSP00000404945.1:p.Gly76Cys
ENST00000466602.1:n.235G>T
ENST00000494263.5:n.660G>T
NM_000784.3:c.226G>T NP_000775.1:p.Gly76Cys
XM_017003488.2:c.-4G>T XP_016858977.1:n.-4G>T
NM_000784.4:c.226G>T MANE Select NP_000775.1:p.Gly76Cys
Search 100 bp 5'
Search 100 bp 3'