Canonical Allele Identifier: CA65813816
Gene: CYP27A1 HGNC NCBI

Linked Data

dbSNP Id: rs557106671
gnomAD v3: 2-218782513-G-T
gnomAD v4: 2-218782513-G-T
MyVariant Identifiers: chr2:g.219647236G>T (hg19) chr2:g.218782513G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218782513G>T , CM000664.2:g.218782513G>T GRCh38
NC_000002.11:g.219647236G>T , CM000664.1:g.219647236G>T GRCh37
NC_000002.10:g.219355480G>T NCBI36
NG_007959.1:g.5765G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258415.9:c.255+76G>T MANE Select ENSP00000258415.4:n.255+76G>T
ENST00000258415.8:c.255+76G>T ENSP00000258415.4:n.255+76G>T
ENST00000445971.1:c.255+76G>T ENSP00000404945.1:n.255+76G>T
ENST00000466602.1:n.264+76G>T
ENST00000494263.5:n.689+76G>T
NM_000784.3:c.255+76G>T NP_000775.1:n.255+76G>T
XM_017003488.2:c.26+76G>T XP_016858977.1:n.26+76G>T
NM_000784.4:c.255+76G>T MANE Select NP_000775.1:n.255+76G>T
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