Canonical Allele Identifier: CA324677739
Gene: CYP2D6 HGNC NCBI
dbSNP:
28439297
gnomAD v3:
22:42132851 T / C
gnomAD v4:
chr22-42132851-T-C
Joint Max Group AF 0.68106713 (EAS)
Genomes Max Group AF 0.67213961 (EAS)
Exomes Max Group AF 0.73910651 (EAS)
MyVariant.info:
GRCh38 chr22:g.42132851T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132851T>C , CM000684.2:g.42132851T>C GRCh38
NG_008376.3:g.2141A>G
NG_008376.4:g.2960A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.309T>C
XM_011529967.1:c.-1045-1015A>G XP_011528269.1:n.-1045-1015A>G
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