Canonical Allele Identifier: CA915951490
Gene: CYP2D6 HGNC NCBI

Linked Data

ClinVar Variation Id: 828796
ClinVar RCV Id: RCV001028707
dbSNP Id: rs1602602668
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132479C>T , CM000684.2:g.42132479C>T GRCh38
NC_000022.10:g.42528486C>T , CM000684.1:g.42528486C>T GRCh37
NC_000022.9:g.40858430C>T NCBI36
NG_008376.3:g.2513G>A
NG_008376.4:g.3332G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-643G>A XP_011528269.1:n.-1045-643G>A
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