Canonical Allele Identifier: CA639489168
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1227059025
gnomAD v2: 22-42528080-G-GC
gnomAD v3: 22-42132073-G-GC
gnomAD v4: 22-42132073-G-GC
MyVariant Identifiers: chr22:g.42528080_42528081insC (hg19) chr22:g.42132073_42132074insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132076dup , CM000684.2:g.42132076dup GRCh38
NC_000022.10:g.42528083dup , CM000684.1:g.42528083dup GRCh37
NC_000022.9:g.40858027dup NCBI36
NG_008376.3:g.2918dup
NG_008376.4:g.3737dup

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-238dup XP_011528269.1:n.-1045-238dup
XR_430455.2:n.351dup
XR_002958749.1:n.298dup
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