Canonical Allele Identifier: CA597652491
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1382761548
gnomAD v2: 11-14915600-G-A
gnomAD v3: 11-14894054-G-A
gnomAD v4: 11-14894054-G-A
MyVariant Identifiers: chr11:g.14915600G>A (hg19) chr11:g.14894054G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14894054G>A , CM000673.2:g.14894054G>A GRCh38
NC_000011.9:g.14915600G>A , CM000673.1:g.14915600G>A GRCh37
NC_000011.8:g.14872176G>A NCBI36
NG_007936.1:g.3152C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.3:c.-1810C>T XP_011518200.1:n.-1810C>T
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