Canonical Allele Identifier: CA753326388
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1427898842
MyVariant Identifiers: chr22:g.42126054G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126054G>A , CM000684.2:g.42126054G>A GRCh38
NC_000022.10:g.42522059G>A , CM000684.1:g.42522059G>A GRCh37
NC_000022.9:g.40852003G>A NCBI36
NG_008376.3:g.8938C>T
NG_008376.4:g.9757C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-101C>T XP_011528268.1:n.1453-101C>T
XM_011529967.1:c.1453-101C>T XP_011528269.1:n.1453-101C>T
XM_011529968.1:c.1453-127C>T XP_011528270.1:n.1453-127C>T
XM_011529969.1:c.1309-101C>T XP_011528271.1:n.1309-101C>T
XM_011529970.1:c.1300-101C>T XP_011528272.1:n.1300-101C>T