Canonical Allele Identifier: CA411769821

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1930938854
• MyVariant Identifiers: chr22:g.42522614T>G (hg19) ; chr22:g.42126612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126612T>G , CM000684.2:g.42126612T>G	GRCh38
NC_000022.10:g.42522614T>G , CM000684.1:g.42522614T>G	GRCh37
NC_000022.9:g.40852558T>G	NCBI36
NG_008376.3:g.8380A>C
NG_008376.4:g.9199A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1254A>C	ENSP00000353241.6:n.1254A>C
ENST00000645361.2:c.1456A>C MANE Select	ENSP00000496150.1:p.Ser486Arg
ENST00000359033.4:c.1303A>C	ENSP00000351927.4:p.Ser435Arg
ENST00000360124.9:c.1074A>C	ENSP00000353241.5:n.1074A>C
ENST00000360608.9:c.1456A>C	ENSP00000353820.5:p.Ser486Arg
ENST00000389970.7:c.1447A>C	ENSP00000374620.4:p.Ser483Arg
ENST00000488442.1:n.2180A>C
NM_000106.5:c.1456A>C	NP_000097.3:p.Ser486Arg
NM_001025161.2:c.1303A>C	NP_001020332.2:p.Ser435Arg
XM_011529966.1:c.1452+4A>C	XP_011528268.1:n.1452+4A>C
XM_011529967.1:c.1452+4A>C	XP_011528269.1:n.1452+4A>C
XM_011529968.1:c.1452+4A>C	XP_011528270.1:n.1452+4A>C
XM_011529969.1:c.1308+4A>C	XP_011528271.1:n.1308+4A>C
XM_011529970.1:c.1299+4A>C	XP_011528272.1:n.1299+4A>C
XM_011529971.1:c.1312A>C	XP_011528273.1:p.Ser438Arg
NM_000106.6:c.1456A>C MANE Select	NP_000097.3:p.Ser486Arg
NM_001025161.3:c.1303A>C	NP_001020332.2:p.Ser435Arg