Canonical Allele Identifier: CA514705685
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1932561903
MyVariant Identifiers: chr22:g.42528614A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132607A>C , CM000684.2:g.42132607A>C GRCh38
NC_000022.10:g.42528614A>C , CM000684.1:g.42528614A>C GRCh37
NC_000022.9:g.40858558A>C NCBI36
NG_008376.3:g.2385T>G
NG_008376.4:g.3204T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.65A>C
XM_011529967.1:c.-1045-771T>G XP_011528269.1:n.-1045-771T>G