Canonical Allele Identifier: CA674002732
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1368208432
MyVariant Identifiers: chr11:g.14893929G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14893929G>C , CM000673.2:g.14893929G>C GRCh38
NC_000011.9:g.14915475G>C , CM000673.1:g.14915475G>C GRCh37
NC_000011.8:g.14872051G>C NCBI36
NG_007936.1:g.3277C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.1:c.-1685C>G XP_011518200.1:n.-1685C>G
XM_011519898.3:c.-1685C>G XP_011518200.1:n.-1685C>G