Canonical Allele Identifier: CA514705631
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1206863517
MyVariant Identifiers: chr22:g.42528606A>G (hg19) chr22:g.42132599A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132599A>G , CM000684.2:g.42132599A>G GRCh38
NC_000022.10:g.42528606A>G , CM000684.1:g.42528606A>G GRCh37
NC_000022.9:g.40858550A>G NCBI36
NG_008376.3:g.2393T>C
NG_008376.4:g.3212T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.57A>G
XM_011529967.1:c.-1045-763T>C XP_011528269.1:n.-1045-763T>C
Search 100 bp 5'
Search 100 bp 3'