Canonical Allele Identifier: CA753332179
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1298745257
MyVariant Identifiers: chr22:g.42131076C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131076C>T , CM000684.2:g.42131076C>T GRCh38
NC_000022.10:g.42527078C>T , CM000684.1:g.42527078C>T GRCh37
NC_000022.9:g.40857022C>T NCBI36
NG_008376.3:g.3916G>A
NG_008376.4:g.4735G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-285G>A XP_011528268.1:n.-285G>A
XM_011529967.1:c.-285G>A XP_011528269.1:n.-285G>A
XM_011529968.1:c.-285G>A XP_011528270.1:n.-285G>A
XM_011529969.1:c.37+221G>A XP_011528271.1:n.37+221G>A
XM_011529970.1:c.-285G>A XP_011528272.1:n.-285G>A
XM_011529971.1:c.37+221G>A XP_011528273.1:n.37+221G>A
XM_011529972.1:c.-285G>A XP_011528274.1:n.-285G>A
XR_430455.2:n.328+388C>T
XR_002958749.1:n.275+388C>T