Canonical Allele Identifier: CA639489176
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1424163290
gnomAD v2: 22-42528193-T-TACAG
gnomAD v3: 22-42132186-T-TACAG
gnomAD v4: 22-42132186-T-TACAG
MyVariant Identifiers: chr22:g.42528193_42528194insACAG (hg19) chr22:g.42132186_42132187insACAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132187_42132190dup , CM000684.2:g.42132187_42132190dup GRCh38
NC_000022.10:g.42528194_42528197dup , CM000684.1:g.42528194_42528197dup GRCh37
NC_000022.9:g.40858138_40858141dup NCBI36
NG_008376.3:g.2802_2805dup
NG_008376.4:g.3621_3624dup

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-354_-1045-351dup XP_011528269.1:n.-1045-354_-1045-351dup
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