Canonical Allele Identifier: CA1025920344
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs35028622

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126069A>G , CM000684.2:g.42126069A>G GRCh38
NG_008376.3:g.8923T>C
NG_008376.4:g.9742T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-116T>C XP_011528268.1:n.1453-116T>C
XM_011529967.1:c.1453-116T>C XP_011528269.1:n.1453-116T>C
XM_011529968.1:c.1453-142T>C XP_011528270.1:n.1453-142T>C
XM_011529969.1:c.1309-116T>C XP_011528271.1:n.1309-116T>C
XM_011529970.1:c.1300-116T>C XP_011528272.1:n.1300-116T>C