Canonical Allele Identifier: CA411773990

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128891-C-A
• MyVariant Identifiers: chr22:g.42524893C>A (hg19) ; chr22:g.42128891C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128891C>A , CM000684.2:g.42128891C>A	GRCh38
NC_000022.10:g.42524893C>A , CM000684.1:g.42524893C>A	GRCh37
NC_000022.9:g.40854837C>A	NCBI36
NG_008376.3:g.6101G>T
NG_008376.4:g.6920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.406G>T	ENSP00000353241.6:p.Ala136Ser
ENST00000645361.2:c.559G>T MANE Select	ENSP00000496150.1:p.Ala187Ser
ENST00000359033.4:c.406G>T	ENSP00000351927.4:p.Ala136Ser
ENST00000360124.9:c.226G>T	ENSP00000353241.5:p.Ala76Ser
ENST00000360608.9:c.559G>T	ENSP00000353820.5:p.Ala187Ser
ENST00000389970.7:c.493G>T	ENSP00000374620.4:p.Ala165Ser
ENST00000488442.1:n.1283G>T
NM_000106.5:c.559G>T	NP_000097.3:p.Ala187Ser
NM_001025161.2:c.406G>T	NP_001020332.2:p.Ala136Ser
XM_011529966.1:c.559G>T	XP_011528268.1:p.Ala187Ser
XM_011529967.1:c.559G>T	XP_011528269.1:p.Ala187Ser
XM_011529968.1:c.559G>T	XP_011528270.1:p.Ala187Ser
XM_011529969.1:c.415G>T	XP_011528271.1:p.Ala139Ser
XM_011529970.1:c.406G>T	XP_011528272.1:p.Ala136Ser
XM_011529971.1:c.415G>T	XP_011528273.1:p.Ala139Ser
XM_011529972.1:c.559G>T	XP_011528274.1:p.Ala187Ser
NM_000106.6:c.559G>T MANE Select	NP_000097.3:p.Ala187Ser
NM_001025161.3:c.406G>T	NP_001020332.2:p.Ala136Ser