Canonical Allele Identifier: CA1025920351
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1930837148

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126072T>C , CM000684.2:g.42126072T>C GRCh38
NC_000022.10:g.42522077T>C , CM000684.1:g.42522077T>C GRCh37
NC_000022.9:g.40852021T>C NCBI36
NG_008376.3:g.8920A>G
NG_008376.4:g.9739A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-119A>G XP_011528268.1:n.1453-119A>G
XM_011529967.1:c.1453-119A>G XP_011528269.1:n.1453-119A>G
XM_011529968.1:c.1453-145A>G XP_011528270.1:n.1453-145A>G
XM_011529969.1:c.1309-119A>G XP_011528271.1:n.1309-119A>G
XM_011529970.1:c.1300-119A>G XP_011528272.1:n.1300-119A>G