Canonical Allele Identifier: CA674002580
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1400457189
MyVariant Identifiers: chr11:g.14893712C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14893712C>T , CM000673.2:g.14893712C>T GRCh38
NC_000011.9:g.14915258C>T , CM000673.1:g.14915258C>T GRCh37
NC_000011.8:g.14871834C>T NCBI36
NG_007936.1:g.3494G>A

Transcript Alleles

HGVS Amino-acid change
XM_011519898.1:c.-1468G>A XP_011518200.1:n.-1468G>A
XM_011519898.3:c.-1468G>A XP_011518200.1:n.-1468G>A