Canonical Allele Identifier: CA514705566
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1932557232
gnomAD v4: 22-42132588-C-T
MyVariant Identifiers: chr22:g.42528595C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132588C>T , CM000684.2:g.42132588C>T GRCh38
NC_000022.10:g.42528595C>T , CM000684.1:g.42528595C>T GRCh37
NC_000022.9:g.40858539C>T NCBI36
NG_008376.3:g.2404G>A
NG_008376.4:g.3223G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.46C>T
XM_011529967.1:c.-1045-752G>A XP_011528269.1:n.-1045-752G>A
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