Canonical Allele Identifier: CA217908558
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs369432314
gnomAD v2: 11-14915769-C-T
gnomAD v3: 11-14894223-C-T
gnomAD v4: 11-14894223-C-T
MyVariant Identifiers: chr11:g.14915769C>T (hg19) chr11:g.14894223C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14894223C>T , CM000673.2:g.14894223C>T GRCh38
NC_000011.9:g.14915769C>T , CM000673.1:g.14915769C>T GRCh37
NC_000011.8:g.14872345C>T NCBI36
NG_007936.1:g.2983G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.3:c.-1979G>A XP_011518200.1:n.-1979G>A
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