Canonical Allele Identifier: CA514706622
Gene: CYP2D6 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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