Canonical Allele Identifier: CA514705637
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1438009443
MyVariant Identifiers: chr22:g.42528607C>G (hg19) chr22:g.42132600C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132600C>G , CM000684.2:g.42132600C>G GRCh38
NC_000022.10:g.42528607C>G , CM000684.1:g.42528607C>G GRCh37
NC_000022.9:g.40858551C>G NCBI36
NG_008376.3:g.2392G>C
NG_008376.4:g.3211G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.58C>G
XM_011529967.1:c.-1045-764G>C XP_011528269.1:n.-1045-764G>C
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