Canonical Allele Identifier: CA915951484
Gene: CYP2D6 HGNC NCBI

Linked Data

ClinVar Variation Id: 828804
ClinVar RCV Id: RCV001028715
dbSNP Id: rs1602600410
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132154T>C , CM000684.2:g.42132154T>C GRCh38
NC_000022.10:g.42528161T>C , CM000684.1:g.42528161T>C GRCh37
NC_000022.9:g.40858105T>C NCBI36
NG_008376.3:g.2838A>G
NG_008376.4:g.3657A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-318A>G XP_011528269.1:n.-1045-318A>G
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