Canonical Allele Identifier: CA10264775
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs758475046

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127906C>T , CM000684.2:g.42127906C>T GRCh38
NC_000022.10:g.42523908C>T , CM000684.1:g.42523908C>T GRCh37
NC_000022.9:g.40853852C>T NCBI36
NG_008376.3:g.7086G>A
NG_008376.4:g.7905G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.719G>A ENSP00000353241.6:p.Trp240Ter
ENST00000645361.2:c.921G>A MANE Select ENSP00000496150.1:p.Met307Ile
ENST00000359033.4:c.768G>A ENSP00000351927.4:p.Met256Ile
ENST00000360124.9:c.539G>A ENSP00000353241.5:p.Trp180Ter
ENST00000360608.9:c.921G>A ENSP00000353820.5:p.Met307Ile
ENST00000389970.7:c.855G>A ENSP00000374620.4:p.Met285Ile
ENST00000488442.1:n.1645G>A
NM_000106.5:c.921G>A NP_000097.3:p.Met307Ile
NM_001025161.2:c.768G>A NP_001020332.2:p.Met256Ile
XM_011529966.1:c.921G>A XP_011528268.1:p.Met307Ile
XM_011529967.1:c.921G>A XP_011528269.1:p.Met307Ile
XM_011529968.1:c.921G>A XP_011528270.1:p.Met307Ile
XM_011529969.1:c.777G>A XP_011528271.1:p.Met259Ile
XM_011529970.1:c.768G>A XP_011528272.1:p.Met256Ile
XM_011529971.1:c.777G>A XP_011528273.1:p.Met259Ile
XM_011529972.1:c.843+268G>A XP_011528274.1:n.843+268G>A
NM_000106.6:c.921G>A MANE Select NP_000097.3:p.Met307Ile
NM_001025161.3:c.768G>A NP_001020332.2:p.Met256Ile