Canonical Allele Identifier: CA324677021
Gene: CYP2D6 HGNC NCBI
dbSNP:
59099247
gnomAD v2:
22:42528096 C / T
gnomAD v3:
22:42132089 C / T
gnomAD v4:
chr22-42132089-C-T
Joint Max Group AF 0.07652499 (AFR)
Genomes Max Group AF 0.07652499 (AFR)
MyVariant.info:
GRCh38 chr22:g.42132089C>T
GRCh37 chr22:g.42528096C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132089C>T , CM000684.2:g.42132089C>T GRCh38
NC_000022.10:g.42528096C>T , CM000684.1:g.42528096C>T GRCh37
NC_000022.9:g.40858040C>T NCBI36
NG_008376.3:g.2903G>A
NG_008376.4:g.3722G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-253G>A XP_011528269.1:n.-1045-253G>A
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