Canonical Allele Identifier: CA10264634
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs773062931

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127490A>T , CM000684.2:g.42127490A>T GRCh38
NC_000022.10:g.42523492A>T , CM000684.1:g.42523492A>T GRCh37
NC_000022.9:g.40853436A>T NCBI36
NG_008376.3:g.7502T>A
NG_008376.4:g.8321T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.928T>A ENSP00000353241.6:n.928T>A
ENST00000645361.2:c.1130T>A MANE Select ENSP00000496150.1:p.Met377Lys
ENST00000359033.4:c.977T>A ENSP00000351927.4:p.Met326Lys
ENST00000360124.9:c.748T>A ENSP00000353241.5:n.748T>A
ENST00000360608.9:c.1130T>A ENSP00000353820.5:p.Met377Lys
ENST00000389970.7:c.1121T>A ENSP00000374620.4:p.Met374Lys
ENST00000488442.1:n.1854T>A
NM_000106.5:c.1130T>A NP_000097.3:p.Met377Lys
NM_001025161.2:c.977T>A NP_001020332.2:p.Met326Lys
XM_011529966.1:c.1130T>A XP_011528268.1:p.Met377Lys
XM_011529967.1:c.1130T>A XP_011528269.1:p.Met377Lys
XM_011529968.1:c.1130T>A XP_011528270.1:p.Met377Lys
XM_011529969.1:c.986T>A XP_011528271.1:p.Met329Lys
XM_011529970.1:c.977T>A XP_011528272.1:p.Met326Lys
XM_011529971.1:c.986T>A XP_011528273.1:p.Met329Lys
NM_000106.6:c.1130T>A MANE Select NP_000097.3:p.Met377Lys
NM_001025161.3:c.977T>A NP_001020332.2:p.Met326Lys