Canonical Allele Identifier: CA411772965

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524174A>G (hg19) ; chr22:g.42128172A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128172A>G , CM000684.2:g.42128172A>G	GRCh38
NC_000022.10:g.42524174A>G , CM000684.1:g.42524174A>G	GRCh37
NC_000022.9:g.40854118A>G	NCBI36
NG_008376.3:g.6820T>C
NG_008376.4:g.7639T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.690+2T>C	ENSP00000353241.6:n.690+2T>C
ENST00000645361.2:c.843+2T>C MANE Select	ENSP00000496150.1:n.843+2T>C
ENST00000359033.4:c.690+2T>C	ENSP00000351927.4:n.690+2T>C
ENST00000360124.9:c.510+2T>C	ENSP00000353241.5:n.510+2T>C
ENST00000360608.9:c.843+2T>C	ENSP00000353820.5:n.843+2T>C
ENST00000389970.7:c.777+2T>C	ENSP00000374620.4:n.777+2T>C
ENST00000488442.1:n.1567+2T>C
NM_000106.5:c.843+2T>C	NP_000097.3:n.843+2T>C
NM_001025161.2:c.690+2T>C	NP_001020332.2:n.690+2T>C
XM_011529966.1:c.843+2T>C	XP_011528268.1:n.843+2T>C
XM_011529967.1:c.843+2T>C	XP_011528269.1:n.843+2T>C
XM_011529968.1:c.843+2T>C	XP_011528270.1:n.843+2T>C
XM_011529969.1:c.699+2T>C	XP_011528271.1:n.699+2T>C
XM_011529970.1:c.690+2T>C	XP_011528272.1:n.690+2T>C
XM_011529971.1:c.699+2T>C	XP_011528273.1:n.699+2T>C
XM_011529972.1:c.843+2T>C	XP_011528274.1:n.843+2T>C
NM_000106.6:c.843+2T>C MANE Select	NP_000097.3:n.843+2T>C
NM_001025161.3:c.690+2T>C	NP_001020332.2:n.690+2T>C