Canonical Allele Identifier: CA674002870
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1418382000
MyVariant Identifiers: chr11:g.14894052A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14894052A>G , CM000673.2:g.14894052A>G GRCh38
NC_000011.9:g.14915598A>G , CM000673.1:g.14915598A>G GRCh37
NC_000011.8:g.14872174A>G NCBI36
NG_007936.1:g.3154T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.3:c.-1808T>C XP_011518200.1:n.-1808T>C