Canonical Allele Identifier: CA514705727
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1932564854
MyVariant Identifiers: chr22:g.42528621G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132614G>A , CM000684.2:g.42132614G>A GRCh38
NC_000022.10:g.42528621G>A , CM000684.1:g.42528621G>A GRCh37
NC_000022.9:g.40858565G>A NCBI36
NG_008376.3:g.2378C>T
NG_008376.4:g.3197C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.72G>A
XM_011529967.1:c.-1045-778C>T XP_011528269.1:n.-1045-778C>T
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