Canonical Allele Identifier: CA753333120
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1395664634
MyVariant Identifiers: chr22:g.42132338C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132338C>G , CM000684.2:g.42132338C>G GRCh38
NC_000022.10:g.42528345C>G , CM000684.1:g.42528345C>G GRCh37
NC_000022.9:g.40858289C>G NCBI36
NG_008376.3:g.2654G>C
NG_008376.4:g.3473G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011529967.1:c.-1045-502G>C XP_011528269.1:n.-1045-502G>C