Canonical Allele Identifier: CA2406581157
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1960456670
gnomAD v4: 22-42131050-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131050A>C , CM000684.2:g.42131050A>C GRCh38
NC_000022.10:g.42527052A>C , CM000684.1:g.42527052A>C GRCh37
NC_000022.9:g.40856996A>C NCBI36
NG_008376.3:g.3942T>G
NG_008376.4:g.4761T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-259T>G XP_011528268.1:n.-259T>G
XM_011529967.1:c.-259T>G XP_011528269.1:n.-259T>G
XM_011529968.1:c.-259T>G XP_011528270.1:n.-259T>G
XM_011529969.1:c.37+247T>G XP_011528271.1:n.37+247T>G
XM_011529970.1:c.-259T>G XP_011528272.1:n.-259T>G
XM_011529971.1:c.37+247T>G XP_011528273.1:n.37+247T>G
XM_011529972.1:c.-259T>G XP_011528274.1:n.-259T>G
XR_430455.2:n.328+362A>C
XR_002958749.1:n.275+362A>C
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