Canonical Allele Identifier: CA411774144

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1353497796
• MyVariant Identifiers: chr22:g.42524940G>C (hg19) ; chr22:g.42128938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128938G>C , CM000684.2:g.42128938G>C	GRCh38
NC_000022.10:g.42524940G>C , CM000684.1:g.42524940G>C	GRCh37
NC_000022.9:g.40854884G>C	NCBI36
NG_008376.3:g.6054C>G
NG_008376.4:g.6873C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.359C>G	ENSP00000353241.6:p.Pro120Arg
ENST00000645361.2:c.512C>G MANE Select	ENSP00000496150.1:p.Pro171Arg
ENST00000359033.4:c.359C>G	ENSP00000351927.4:p.Pro120Arg
ENST00000360124.9:c.179C>G	ENSP00000353241.5:p.Pro60Arg
ENST00000360608.9:c.512C>G	ENSP00000353820.5:p.Pro171Arg
ENST00000389970.7:c.446C>G	ENSP00000374620.4:p.Pro149Arg
ENST00000488442.1:n.1236C>G
NM_000106.5:c.512C>G	NP_000097.3:p.Pro171Arg
NM_001025161.2:c.359C>G	NP_001020332.2:p.Pro120Arg
XM_011529966.1:c.512C>G	XP_011528268.1:p.Pro171Arg
XM_011529967.1:c.512C>G	XP_011528269.1:p.Pro171Arg
XM_011529968.1:c.512C>G	XP_011528270.1:p.Pro171Arg
XM_011529969.1:c.368C>G	XP_011528271.1:p.Pro123Arg
XM_011529970.1:c.359C>G	XP_011528272.1:p.Pro120Arg
XM_011529971.1:c.368C>G	XP_011528273.1:p.Pro123Arg
XM_011529972.1:c.512C>G	XP_011528274.1:p.Pro171Arg
NM_000106.6:c.512C>G MANE Select	NP_000097.3:p.Pro171Arg
NM_001025161.3:c.359C>G	NP_001020332.2:p.Pro120Arg