Canonical Allele Identifier: CA915951492
Gene: CYP2D6 HGNC NCBI

Linked Data

ClinVar Variation Id: 829609
ClinVar RCV Id: RCV001029534
dbSNP Id: rs1602602990

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132522T>C , CM000684.2:g.42132522T>C GRCh38
NC_000022.10:g.42528529T>C , CM000684.1:g.42528529T>C GRCh37
NC_000022.9:g.40858473T>C NCBI36
NG_008376.3:g.2470A>G
NG_008376.4:g.3289A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-686A>G XP_011528269.1:n.-1045-686A>G