Canonical Allele Identifier: CA514705487
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42528583A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132576A>C , CM000684.2:g.42132576A>C GRCh38
NC_000022.10:g.42528583A>C , CM000684.1:g.42528583A>C GRCh37
NC_000022.9:g.40858527A>C NCBI36
NG_008376.3:g.2416T>G
NG_008376.4:g.3235T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.34A>C
XM_011529967.1:c.-1045-740T>G XP_011528269.1:n.-1045-740T>G
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