Canonical Allele Identifier: CA65813823
Gene: CYP27A1 HGNC NCBI

Linked Data

dbSNP Id: rs546155967
gnomAD v3: 2-218782547-G-A
gnomAD v4: 2-218782547-G-A
MyVariant Identifiers: chr2:g.219647270G>A (hg19) chr2:g.218782547G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218782547G>A , CM000664.2:g.218782547G>A GRCh38
NC_000002.11:g.219647270G>A , CM000664.1:g.219647270G>A GRCh37
NC_000002.10:g.219355514G>A NCBI36
NG_007959.1:g.5799G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.255+110G>A MANE Select ENSP00000258415.4:n.255+110G>A
ENST00000258415.8:c.255+110G>A ENSP00000258415.4:n.255+110G>A
ENST00000445971.1:c.255+110G>A ENSP00000404945.1:n.255+110G>A
ENST00000466602.1:n.264+110G>A
ENST00000494263.5:n.689+110G>A
NM_000784.3:c.255+110G>A NP_000775.1:n.255+110G>A
XM_017003488.2:c.26+110G>A XP_016858977.1:n.26+110G>A
NM_000784.4:c.255+110G>A MANE Select NP_000775.1:n.255+110G>A
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