Canonical Allele Identifier: CA411774647

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42525086A>G (hg19) ; chr22:g.42129084A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129084A>G , CM000684.2:g.42129084A>G	GRCh38
NC_000022.10:g.42525086A>G , CM000684.1:g.42525086A>G	GRCh37
NC_000022.9:g.40855030A>G	NCBI36
NG_008376.3:g.5908T>C
NG_008376.4:g.6727T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.353-140T>C	ENSP00000353241.6:n.353-140T>C
ENST00000645361.2:c.454T>C MANE Select	ENSP00000496150.1:p.Trp152Arg
ENST00000359033.4:c.353-140T>C	ENSP00000351927.4:n.353-140T>C
ENST00000360124.9:c.173-140T>C	ENSP00000353241.5:n.173-140T>C
ENST00000360608.9:c.454T>C	ENSP00000353820.5:p.Trp152Arg
ENST00000389970.7:c.388T>C	ENSP00000374620.4:p.Trp130Arg
ENST00000488442.1:n.1178T>C
NM_000106.5:c.454T>C	NP_000097.3:p.Trp152Arg
NM_001025161.2:c.353-140T>C	NP_001020332.2:n.353-140T>C
XM_011529966.1:c.454T>C	XP_011528268.1:p.Trp152Arg
XM_011529967.1:c.454T>C	XP_011528269.1:p.Trp152Arg
XM_011529968.1:c.454T>C	XP_011528270.1:p.Trp152Arg
XM_011529969.1:c.311T>C	XP_011528271.1:p.Val104Ala
XM_011529970.1:c.353-140T>C	XP_011528272.1:n.353-140T>C
XM_011529971.1:c.311T>C	XP_011528273.1:p.Val104Ala
XM_011529972.1:c.454T>C	XP_011528274.1:p.Trp152Arg
NM_000106.6:c.454T>C MANE Select	NP_000097.3:p.Trp152Arg
NM_001025161.3:c.353-140T>C	NP_001020332.2:n.353-140T>C