Canonical Allele Identifier: CA10264513
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs28371736

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126619G>C , CM000684.2:g.42126619G>C GRCh38
NC_000022.10:g.42522621G>C , CM000684.1:g.42522621G>C GRCh37
NC_000022.9:g.40852565G>C NCBI36
NG_008376.3:g.8373C>G
NG_008376.4:g.9192C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1247C>G ENSP00000353241.6:n.1247C>G
ENST00000645361.2:c.1449C>G MANE Select ENSP00000496150.1:p.Phe483Leu
ENST00000359033.4:c.1296C>G ENSP00000351927.4:p.Phe432Leu
ENST00000360124.9:c.1067C>G ENSP00000353241.5:n.1067C>G
ENST00000360608.9:c.1449C>G ENSP00000353820.5:p.Phe483Leu
ENST00000389970.7:c.1440C>G ENSP00000374620.4:p.Phe480Leu
ENST00000488442.1:n.2173C>G
NM_000106.5:c.1449C>G NP_000097.3:p.Phe483Leu
NM_001025161.2:c.1296C>G NP_001020332.2:p.Phe432Leu
XM_011529966.1:c.1449C>G XP_011528268.1:p.Phe483Leu
XM_011529967.1:c.1449C>G XP_011528269.1:p.Phe483Leu
XM_011529968.1:c.1449C>G XP_011528270.1:p.Phe483Leu
XM_011529969.1:c.1305C>G XP_011528271.1:p.Phe435Leu
XM_011529970.1:c.1296C>G XP_011528272.1:p.Phe432Leu
XM_011529971.1:c.1305C>G XP_011528273.1:p.Phe435Leu
NM_000106.6:c.1449C>G MANE Select NP_000097.3:p.Phe483Leu
NM_001025161.3:c.1296C>G NP_001020332.2:p.Phe432Leu