Canonical Allele Identifier: CA514706079
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42528679C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132672C>A , CM000684.2:g.42132672C>A GRCh38
NC_000022.10:g.42528679C>A , CM000684.1:g.42528679C>A GRCh37
NC_000022.9:g.40858623C>A NCBI36
NG_008376.3:g.2320G>T
NG_008376.4:g.3139G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.130C>A
XM_011529967.1:c.-1045-836G>T XP_011528269.1:n.-1045-836G>T