Canonical Allele Identifier: CA753333052
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1185302651
MyVariant Identifiers: chr22:g.42132195G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132195G>A , CM000684.2:g.42132195G>A GRCh38
NC_000022.10:g.42528202G>A , CM000684.1:g.42528202G>A GRCh37
NC_000022.9:g.40858146G>A NCBI36
NG_008376.3:g.2797C>T
NG_008376.4:g.3616C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-359C>T XP_011528269.1:n.-1045-359C>T