Canonical Allele Identifier: CA514706474
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42528745A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132738A>T , CM000684.2:g.42132738A>T GRCh38
NC_000022.10:g.42528745A>T , CM000684.1:g.42528745A>T GRCh37
NC_000022.9:g.40858689A>T NCBI36
NG_008376.3:g.2254T>A
NG_008376.4:g.3073T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.196A>T
XM_011529967.1:c.-1045-902T>A XP_011528269.1:n.-1045-902T>A
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