Canonical Allele Identifier: CA411774777

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42525149G>C (hg19) ; chr22:g.42129147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129147G>C , CM000684.2:g.42129147G>C	GRCh38
NC_000022.10:g.42525149G>C , CM000684.1:g.42525149G>C	GRCh37
NC_000022.9:g.40855093G>C	NCBI36
NG_008376.3:g.5845C>G
NG_008376.4:g.6664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-203C>G	ENSP00000353241.6:n.353-203C>G
ENST00000645361.2:c.391C>G MANE Select	ENSP00000496150.1:p.Gln131Glu
ENST00000359033.4:c.353-203C>G	ENSP00000351927.4:n.353-203C>G
ENST00000360124.9:c.173-203C>G	ENSP00000353241.5:n.173-203C>G
ENST00000360608.9:c.391C>G	ENSP00000353820.5:p.Gln131Glu
ENST00000389970.7:c.325C>G	ENSP00000374620.4:p.Gln109Glu
ENST00000488442.1:n.1115C>G
NM_000106.5:c.391C>G	NP_000097.3:p.Gln131Glu
NM_001025161.2:c.353-203C>G	NP_001020332.2:n.353-203C>G
XM_011529966.1:c.391C>G	XP_011528268.1:p.Gln131Glu
XM_011529967.1:c.391C>G	XP_011528269.1:p.Gln131Glu
XM_011529968.1:c.391C>G	XP_011528270.1:p.Gln131Glu
XM_011529969.1:c.248C>G	XP_011528271.1:p.Ala83Gly
XM_011529970.1:c.353-203C>G	XP_011528272.1:n.353-203C>G
XM_011529971.1:c.248C>G	XP_011528273.1:p.Ala83Gly
XM_011529972.1:c.391C>G	XP_011528274.1:p.Gln131Glu
NM_000106.6:c.391C>G MANE Select	NP_000097.3:p.Gln131Glu
NM_001025161.3:c.353-203C>G	NP_001020332.2:n.353-203C>G