Canonical Allele Identifier: CA753333138
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1080985
MyVariant Identifiers: chr22:g.42132375G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132375G>A , CM000684.2:g.42132375G>A GRCh38
NG_008376.3:g.2617C>T
NG_008376.4:g.3436C>T

Transcript Alleles

HGVS Amino-acid change
XM_011529967.1:c.-1045-539C>T XP_011528269.1:n.-1045-539C>T