Canonical Allele Identifier: CA411772574

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146932910
• MyVariant Identifiers: chr22:g.42523904T>A (hg19) ; chr22:g.42127902T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127902T>A , CM000684.2:g.42127902T>A	GRCh38
NC_000022.10:g.42523904T>A , CM000684.1:g.42523904T>A	GRCh37
NC_000022.9:g.40853848T>A	NCBI36
NG_008376.3:g.7090A>T
NG_008376.4:g.7909A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.723A>T	ENSP00000353241.6:p.Ter241Cys
ENST00000645361.2:c.925A>T MANE Select	ENSP00000496150.1:p.Thr309Ser
ENST00000359033.4:c.772A>T	ENSP00000351927.4:p.Thr258Ser
ENST00000360124.9:c.543A>T	ENSP00000353241.5:p.Ter181Cys
ENST00000360608.9:c.925A>T	ENSP00000353820.5:p.Thr309Ser
ENST00000389970.7:c.859A>T	ENSP00000374620.4:p.Thr287Ser
ENST00000488442.1:n.1649A>T
NM_000106.5:c.925A>T	NP_000097.3:p.Thr309Ser
NM_001025161.2:c.772A>T	NP_001020332.2:p.Thr258Ser
XM_011529966.1:c.925A>T	XP_011528268.1:p.Thr309Ser
XM_011529967.1:c.925A>T	XP_011528269.1:p.Thr309Ser
XM_011529968.1:c.925A>T	XP_011528270.1:p.Thr309Ser
XM_011529969.1:c.781A>T	XP_011528271.1:p.Thr261Ser
XM_011529970.1:c.772A>T	XP_011528272.1:p.Thr258Ser
XM_011529971.1:c.781A>T	XP_011528273.1:p.Thr261Ser
XM_011529972.1:c.844-268A>T	XP_011528274.1:n.844-268A>T
NM_000106.6:c.925A>T MANE Select	NP_000097.3:p.Thr309Ser
NM_001025161.3:c.772A>T	NP_001020332.2:p.Thr258Ser