Canonical Allele Identifier: CA674002565
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1284386290
MyVariant Identifiers: chr11:g.14893693A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14893693A>C , CM000673.2:g.14893693A>C GRCh38
NC_000011.9:g.14915239A>C , CM000673.1:g.14915239A>C GRCh37
NC_000011.8:g.14871815A>C NCBI36
NG_007936.1:g.3513T>G

Transcript Alleles

HGVS Amino-acid change
XM_011519898.1:c.-1449T>G XP_011518200.1:n.-1449T>G
XM_011519898.3:c.-1449T>G XP_011518200.1:n.-1449T>G