Canonical Allele Identifier: CA324677422
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs990084913
gnomAD v4: 22-42132562-G-A
MyVariant Identifiers: chr22:g.42528569G>A (hg19) chr22:g.42132562G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132562G>A , CM000684.2:g.42132562G>A GRCh38
NC_000022.10:g.42528569G>A , CM000684.1:g.42528569G>A GRCh37
NC_000022.9:g.40858513G>A NCBI36
NG_008376.3:g.2430C>T
NG_008376.4:g.3249C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.20G>A
XM_011529967.1:c.-1045-726C>T XP_011528269.1:n.-1045-726C>T
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