Canonical Allele Identifier: CA915951394

Gene: CYP2D6

Linked Data

• ClinVar Variation Id: 828912
• ClinVar RCV Id: RCV001028826
• dbSNP Id: rs1602563686

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126233A>G , CM000684.2:g.42126233A>G	GRCh38
NC_000022.10:g.42522235A>G , CM000684.1:g.42522235A>G	GRCh37
NC_000022.9:g.40852179A>G	NCBI36
NG_008376.3:g.8759T>C
NG_008376.4:g.9578T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.1453-280T>C	XP_011528268.1:n.1453-280T>C
XM_011529967.1:c.1453-280T>C	XP_011528269.1:n.1453-280T>C
XM_011529968.1:c.1453-306T>C	XP_011528270.1:n.1453-306T>C
XM_011529969.1:c.1309-280T>C	XP_011528271.1:n.1309-280T>C
XM_011529970.1:c.1300-280T>C	XP_011528272.1:n.1300-280T>C