Canonical Allele Identifier: CA915951395
Gene: CYP2D6 HGNC NCBI

Linked Data

ClinVar Variation Id: 828911
ClinVar RCV Id: RCV001028825
dbSNP Id: rs1602563722
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126242T>A , CM000684.2:g.42126242T>A GRCh38
NC_000022.10:g.42522244T>A , CM000684.1:g.42522244T>A GRCh37
NC_000022.9:g.40852188T>A NCBI36
NG_008376.3:g.8750A>T
NG_008376.4:g.9569A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-289A>T XP_011528268.1:n.1453-289A>T
XM_011529967.1:c.1453-289A>T XP_011528269.1:n.1453-289A>T
XM_011529968.1:c.1453-315A>T XP_011528270.1:n.1453-315A>T
XM_011529969.1:c.1309-289A>T XP_011528271.1:n.1309-289A>T
XM_011529970.1:c.1300-289A>T XP_011528272.1:n.1300-289A>T
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