Canonical Allele Identifier: CA217908452
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs970571296
MyVariant Identifiers: chr11:g.14893660T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14893660T>A , CM000673.2:g.14893660T>A GRCh38
NC_000011.9:g.14915206T>A , CM000673.1:g.14915206T>A GRCh37
NC_000011.8:g.14871782T>A NCBI36
NG_007936.1:g.3546A>T

Transcript Alleles

HGVS Amino-acid change
XM_011519898.1:c.-1416A>T XP_011518200.1:n.-1416A>T
XM_011519898.3:c.-1416A>T XP_011518200.1:n.-1416A>T