Canonical Allele Identifier: CA514706133
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs762779483
MyVariant Identifiers: chr22:g.42528689A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132682A>G , CM000684.2:g.42132682A>G GRCh38
NC_000022.10:g.42528689A>G , CM000684.1:g.42528689A>G GRCh37
NC_000022.9:g.40858633A>G NCBI36
NG_008376.3:g.2310T>C
NG_008376.4:g.3129T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.140A>G
XM_011529967.1:c.-1045-846T>C XP_011528269.1:n.-1045-846T>C