Canonical Allele Identifier: CA411769834

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522622A>G (hg19) ; chr22:g.42126620A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126620A>G , CM000684.2:g.42126620A>G	GRCh38
NC_000022.10:g.42522622A>G , CM000684.1:g.42522622A>G	GRCh37
NC_000022.9:g.40852566A>G	NCBI36
NG_008376.3:g.8372T>C
NG_008376.4:g.9191T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1246T>C	ENSP00000353241.6:n.1246T>C
ENST00000645361.2:c.1448T>C MANE Select	ENSP00000496150.1:p.Phe483Ser
ENST00000359033.4:c.1295T>C	ENSP00000351927.4:p.Phe432Ser
ENST00000360124.9:c.1066T>C	ENSP00000353241.5:n.1066T>C
ENST00000360608.9:c.1448T>C	ENSP00000353820.5:p.Phe483Ser
ENST00000389970.7:c.1439T>C	ENSP00000374620.4:p.Phe480Ser
ENST00000488442.1:n.2172T>C
NM_000106.5:c.1448T>C	NP_000097.3:p.Phe483Ser
NM_001025161.2:c.1295T>C	NP_001020332.2:p.Phe432Ser
XM_011529966.1:c.1448T>C	XP_011528268.1:p.Phe483Ser
XM_011529967.1:c.1448T>C	XP_011528269.1:p.Phe483Ser
XM_011529968.1:c.1448T>C	XP_011528270.1:p.Phe483Ser
XM_011529969.1:c.1304T>C	XP_011528271.1:p.Phe435Ser
XM_011529970.1:c.1295T>C	XP_011528272.1:p.Phe432Ser
XM_011529971.1:c.1304T>C	XP_011528273.1:p.Phe435Ser
NM_000106.6:c.1448T>C MANE Select	NP_000097.3:p.Phe483Ser
NM_001025161.3:c.1295T>C	NP_001020332.2:p.Phe432Ser