Canonical Allele Identifier: CA324676940
Gene: CYP2D6 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.42132026T>C
gnomAD v3:
22:42132026 T / C
gnomAD v4:
chr22-42132026-T-C
Joint Max Group AF 0.05060595 (EAS)
Genomes Max Group AF 0.05060595 (EAS)
dbSNP:
28735595
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132026T>C , CM000684.2:g.42132026T>C GRCh38
NC_000022.10:g.42528033T>C , CM000684.1:g.42528033T>C GRCh37
NC_000022.9:g.40857977T>C NCBI36
NG_008376.3:g.2966A>G
NG_008376.4:g.3785A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-190A>G XP_011528269.1:n.-1045-190A>G
XR_430455.2:n.329-28T>C
XR_002958749.1:n.276-28T>C
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