Canonical Allele Identifier: CA915951393

Gene: CYP2D6

Linked Data

• ClinVar Variation Id: 828913
• ClinVar RCV Id: RCV001028827
• dbSNP Id: rs1602563653

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126211T>C , CM000684.2:g.42126211T>C	GRCh38
NC_000022.10:g.42522213T>C , CM000684.1:g.42522213T>C	GRCh37
NC_000022.9:g.40852157T>C	NCBI36
NG_008376.3:g.8781A>G
NG_008376.4:g.9600A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.1453-258A>G	XP_011528268.1:n.1453-258A>G
XM_011529967.1:c.1453-258A>G	XP_011528269.1:n.1453-258A>G
XM_011529968.1:c.1453-284A>G	XP_011528270.1:n.1453-284A>G
XM_011529969.1:c.1309-258A>G	XP_011528271.1:n.1309-258A>G
XM_011529970.1:c.1300-258A>G	XP_011528272.1:n.1300-258A>G