Canonical Allele Identifier: CA10265160
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs374616348

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129183C>T , CM000684.2:g.42129183C>T GRCh38
NC_000022.10:g.42525185C>T , CM000684.1:g.42525185C>T GRCh37
NC_000022.9:g.40855129C>T NCBI36
NG_008376.3:g.5809G>A
NG_008376.4:g.6628G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.353-239G>A ENSP00000353241.6:n.353-239G>A
ENST00000645361.2:c.355G>A MANE Select ENSP00000496150.1:p.Val119Met
ENST00000359033.4:c.353-239G>A ENSP00000351927.4:n.353-239G>A
ENST00000360124.9:c.173-239G>A ENSP00000353241.5:n.173-239G>A
ENST00000360608.9:c.355G>A ENSP00000353820.5:p.Val119Met
ENST00000389970.7:c.289G>A ENSP00000374620.4:p.Val97Met
ENST00000488442.1:n.1079G>A
NM_000106.5:c.355G>A NP_000097.3:p.Val119Met
NM_001025161.2:c.353-239G>A NP_001020332.2:n.353-239G>A
XM_011529966.1:c.355G>A XP_011528268.1:p.Val119Met
XM_011529967.1:c.355G>A XP_011528269.1:p.Val119Met
XM_011529968.1:c.355G>A XP_011528270.1:p.Val119Met
XM_011529969.1:c.212G>A XP_011528271.1:p.Gly71Asp
XM_011529970.1:c.353-239G>A XP_011528272.1:n.353-239G>A
XM_011529971.1:c.212G>A XP_011528273.1:p.Gly71Asp
XM_011529972.1:c.355G>A XP_011528274.1:p.Val119Met
NM_000106.6:c.355G>A MANE Select NP_000097.3:p.Val119Met
NM_001025161.3:c.353-239G>A NP_001020332.2:n.353-239G>A