Canonical Allele Identifier: CA753333093
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1249431271
MyVariant Identifiers: chr22:g.42132294C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132294C>T , CM000684.2:g.42132294C>T GRCh38
NC_000022.10:g.42528301C>T , CM000684.1:g.42528301C>T GRCh37
NC_000022.9:g.40858245C>T NCBI36
NG_008376.3:g.2698G>A
NG_008376.4:g.3517G>A

Transcript Alleles

HGVS Amino-acid change
XM_011529967.1:c.-1045-458G>A XP_011528269.1:n.-1045-458G>A