Canonical Allele Identifier: CA514705366
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42528563T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132556T>C , CM000684.2:g.42132556T>C GRCh38
NC_000022.10:g.42528563T>C , CM000684.1:g.42528563T>C GRCh37
NC_000022.9:g.40858507T>C NCBI36
NG_008376.3:g.2436A>G
NG_008376.4:g.3255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.14T>C
XM_011529967.1:c.-1045-720A>G XP_011528269.1:n.-1045-720A>G