Canonical Allele Identifier: CA2738249217
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs2146932026

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127678T>A , CM000684.2:g.42127678T>A GRCh38
NC_000022.10:g.42523680T>A , CM000684.1:g.42523680T>A GRCh37
NC_000022.9:g.40853624T>A NCBI36
NG_008376.3:g.7314A>T
NG_008376.4:g.8133A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.784-44A>T ENSP00000353241.6:n.784-44A>T
ENST00000645361.2:c.986-44A>T MANE Select ENSP00000496150.1:n.986-44A>T
ENST00000359033.4:c.833-44A>T ENSP00000351927.4:n.833-44A>T
ENST00000360124.9:c.604-44A>T ENSP00000353241.5:n.604-44A>T
ENST00000360608.9:c.986-44A>T ENSP00000353820.5:n.986-44A>T
ENST00000389970.7:c.949-16A>T ENSP00000374620.4:n.949-16A>T
ENST00000488442.1:n.1710-44A>T
NM_000106.5:c.986-44A>T NP_000097.3:n.986-44A>T
NM_001025161.2:c.833-44A>T NP_001020332.2:n.833-44A>T
XM_011529966.1:c.986-44A>T XP_011528268.1:n.986-44A>T
XM_011529967.1:c.986-44A>T XP_011528269.1:n.986-44A>T
XM_011529968.1:c.986-44A>T XP_011528270.1:n.986-44A>T
XM_011529969.1:c.842-44A>T XP_011528271.1:n.842-44A>T
XM_011529970.1:c.833-44A>T XP_011528272.1:n.833-44A>T
XM_011529971.1:c.842-44A>T XP_011528273.1:n.842-44A>T
XM_011529972.1:c.844-44A>T XP_011528274.1:n.844-44A>T
NM_000106.6:c.986-44A>T MANE Select NP_000097.3:n.986-44A>T
NM_001025161.3:c.833-44A>T NP_001020332.2:n.833-44A>T