Canonical Allele Identifier: CA639489180
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1356333828

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132290C>T , CM000684.2:g.42132290C>T GRCh38
NC_000022.10:g.42528297C>T , CM000684.1:g.42528297C>T GRCh37
NC_000022.9:g.40858241C>T NCBI36
NG_008376.3:g.2702G>A
NG_008376.4:g.3521G>A

Transcript Alleles

HGVS Amino-acid change
XM_011529967.1:c.-1045-454G>A XP_011528269.1:n.-1045-454G>A