Canonical Allele Identifier: CA324676109
Gene: CYP2D6 HGNC NCBI
dbSNP:
34167214
gnomAD v3:
22:42131122 A / C
gnomAD v4:
chr22-42131122-A-C
Joint Max Group AF 0.00000812 (AFR)
Genomes Max Group AF 0.00000812 (AFR)
MyVariant.info:
GRCh38 chr22:g.42131122A>C
GRCh37 chr22:g.42527124A>C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131122A>C , CM000684.2:g.42131122A>C GRCh38
NC_000022.10:g.42527124A>C , CM000684.1:g.42527124A>C GRCh37
NC_000022.9:g.40857068A>C NCBI36
NG_008376.3:g.3870T>G
NG_008376.4:g.4689T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-331T>G XP_011528268.1:n.-331T>G
XM_011529967.1:c.-331T>G XP_011528269.1:n.-331T>G
XM_011529968.1:c.-331T>G XP_011528270.1:n.-331T>G
XM_011529969.1:c.37+175T>G XP_011528271.1:n.37+175T>G
XM_011529970.1:c.-331T>G XP_011528272.1:n.-331T>G
XM_011529971.1:c.37+175T>G XP_011528273.1:n.37+175T>G
XM_011529972.1:c.-331T>G XP_011528274.1:n.-331T>G
XR_430455.2:n.328+434A>C
XR_002958749.1:n.275+434A>C
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