Canonical Allele Identifier: CA324677029
Gene: CYP2D6 HGNC NCBI
dbSNP:
78047908
gnomAD v2:
22:42528124 G / A
gnomAD v3:
22:42132117 G / A
gnomAD v4:
chr22-42132117-G-A
Joint Max Group AF 0.00390888 (AFR)
Genomes Max Group AF 0.00390909 (AFR)
MyVariant.info:
GRCh38 chr22:g.42132117G>A
GRCh37 chr22:g.42528124G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132117G>A , CM000684.2:g.42132117G>A GRCh38
NC_000022.10:g.42528124G>A , CM000684.1:g.42528124G>A GRCh37
NC_000022.9:g.40858068G>A NCBI36
NG_008376.3:g.2875C>T
NG_008376.4:g.3694C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-281C>T XP_011528269.1:n.-1045-281C>T
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