Canonical Allele Identifier: CA10264755
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs79292917

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127852C>T , CM000684.2:g.42127852C>T GRCh38
NC_000022.10:g.42523854C>T , CM000684.1:g.42523854C>T GRCh37
NC_000022.9:g.40853798C>T NCBI36
NG_008376.3:g.7140G>A
NG_008376.4:g.7959G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.773G>A ENSP00000353241.6:n.773G>A
ENST00000645361.2:c.975G>A MANE Select ENSP00000496150.1:p.Pro325=
ENST00000359033.4:c.822G>A ENSP00000351927.4:p.Pro274=
ENST00000360124.9:c.593G>A ENSP00000353241.5:n.593G>A
ENST00000360608.9:c.975G>A ENSP00000353820.5:p.Pro325=
ENST00000389970.7:c.909G>A ENSP00000374620.4:p.Pro303=
ENST00000488442.1:n.1699G>A
NM_000106.5:c.975G>A NP_000097.3:p.Pro325=
NM_001025161.2:c.822G>A NP_001020332.2:p.Pro274=
XM_011529966.1:c.975G>A XP_011528268.1:p.Pro325=
XM_011529967.1:c.975G>A XP_011528269.1:p.Pro325=
XM_011529968.1:c.975G>A XP_011528270.1:p.Pro325=
XM_011529969.1:c.831G>A XP_011528271.1:p.Pro277=
XM_011529970.1:c.822G>A XP_011528272.1:p.Pro274=
XM_011529971.1:c.831G>A XP_011528273.1:p.Pro277=
XM_011529972.1:c.844-218G>A XP_011528274.1:n.844-218G>A
NM_000106.6:c.975G>A MANE Select NP_000097.3:p.Pro325=
NM_001025161.3:c.822G>A NP_001020332.2:p.Pro274=