Canonical Allele Identifier: CA324675923
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1080993
gnomAD v2: 22-42526969-C-T
gnomAD v3: 22-42130967-C-T
gnomAD v4: 22-42130967-C-T
MyVariant Identifiers: chr22:g.42526969C>T (hg19) chr22:g.42130967C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130967C>T , CM000684.2:g.42130967C>T GRCh38
NC_000022.10:g.42526969C>T , CM000684.1:g.42526969C>T GRCh37
NC_000022.9:g.40856913C>T NCBI36
NG_008376.3:g.4025G>A
NG_008376.4:g.4844G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-176G>A XP_011528268.1:n.-176G>A
XM_011529967.1:c.-176G>A XP_011528269.1:n.-176G>A
XM_011529968.1:c.-176G>A XP_011528270.1:n.-176G>A
XM_011529969.1:c.37+330G>A XP_011528271.1:n.37+330G>A
XM_011529970.1:c.-176G>A XP_011528272.1:n.-176G>A
XM_011529971.1:c.37+330G>A XP_011528273.1:n.37+330G>A
XM_011529972.1:c.-176G>A XP_011528274.1:n.-176G>A
XR_430455.2:n.328+279C>T
XR_002958749.1:n.275+279C>T
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