Canonical Allele Identifier: CA753333227
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1419967139
MyVariant Identifiers: chr22:g.42132581_42132583del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132585_42132587del , CM000684.2:g.42132585_42132587del GRCh38
NC_000022.10:g.42528592_42528594del , CM000684.1:g.42528592_42528594del GRCh37
NC_000022.9:g.40858536_40858538del NCBI36
NG_008376.3:g.2409_2411del
NG_008376.4:g.3228_3230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.43_45del
XM_011529967.1:c.-1045-747_-1045-745del XP_011528269.1:n.-1045-747_-1045-745del
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