Canonical Allele Identifier: CA2844608623

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128694T>G , CM000684.2:g.42128694T>G	GRCh38
NC_000022.10:g.42524696T>G , CM000684.1:g.42524696T>G	GRCh37
NC_000022.9:g.40854640T>G	NCBI36
NG_008376.3:g.6298A>C
NG_008376.4:g.7117A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.513+90A>C	ENSP00000353241.6:n.513+90A>C
ENST00000645361.2:c.666+90A>C MANE Select	ENSP00000496150.1:n.666+90A>C
ENST00000359033.4:c.513+90A>C	ENSP00000351927.4:n.513+90A>C
ENST00000360124.9:c.333+90A>C	ENSP00000353241.5:n.333+90A>C
ENST00000360608.9:c.666+90A>C	ENSP00000353820.5:n.666+90A>C
ENST00000389970.7:c.600+90A>C	ENSP00000374620.4:n.600+90A>C
ENST00000488442.1:n.1390+90A>C
NM_000106.5:c.666+90A>C	NP_000097.3:n.666+90A>C
NM_001025161.2:c.513+90A>C	NP_001020332.2:n.513+90A>C
XM_011529966.1:c.666+90A>C	XP_011528268.1:n.666+90A>C
XM_011529967.1:c.666+90A>C	XP_011528269.1:n.666+90A>C
XM_011529968.1:c.666+90A>C	XP_011528270.1:n.666+90A>C
XM_011529969.1:c.522+90A>C	XP_011528271.1:n.522+90A>C
XM_011529970.1:c.513+90A>C	XP_011528272.1:n.513+90A>C
XM_011529971.1:c.522+90A>C	XP_011528273.1:n.522+90A>C
XM_011529972.1:c.666+90A>C	XP_011528274.1:n.666+90A>C
NM_000106.6:c.666+90A>C MANE Select	NP_000097.3:n.666+90A>C
NM_001025161.3:c.513+90A>C	NP_001020332.2:n.513+90A>C