Canonical Allele Identifier: CA324677634
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1030277730

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132749G>A , CM000684.2:g.42132749G>A GRCh38
NC_000022.10:g.42528756G>A , CM000684.1:g.42528756G>A GRCh37
NC_000022.9:g.40858700G>A NCBI36
NG_008376.3:g.2243C>T
NG_008376.4:g.3062C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.207G>A
XM_011529967.1:c.-1045-913C>T XP_011528269.1:n.-1045-913C>T