Canonical Allele Identifier: CA324676370
Gene: CYP2D6 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.42131469C>T
gnomAD v3:
22:42131469 C / T
gnomAD v4:
chr22-42131469-C-T
Joint Max Group AF 0.37542385 (MID)
Genomes Max Group AF 0.35832129 (SAS)
dbSNP:
28633410
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131469C>T , CM000684.2:g.42131469C>T GRCh38
NG_008376.3:g.3523G>A
NG_008376.4:g.4342G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-678G>A XP_011528268.1:n.-678G>A
XM_011529967.1:c.-678G>A XP_011528269.1:n.-678G>A
XM_011529968.1:c.-678G>A XP_011528270.1:n.-678G>A
XM_011529969.1:c.-136G>A XP_011528271.1:n.-136G>A
XM_011529970.1:c.-678G>A XP_011528272.1:n.-678G>A
XM_011529971.1:c.-136G>A XP_011528273.1:n.-136G>A
XM_011529972.1:c.-678G>A XP_011528274.1:n.-678G>A
XR_430455.2:n.329-585C>T
XR_002958749.1:n.276-585C>T
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