Canonical Allele Identifier: CA514706624
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42528769G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132762G>T , CM000684.2:g.42132762G>T GRCh38
NC_000022.10:g.42528769G>T , CM000684.1:g.42528769G>T GRCh37
NC_000022.9:g.40858713G>T NCBI36
NG_008376.3:g.2230C>A
NG_008376.4:g.3049C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.220G>T
XM_011529967.1:c.-1045-926C>A XP_011528269.1:n.-1045-926C>A