Canonical Allele Identifier: CA411773567

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524325G>C (hg19) ; chr22:g.42128323G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128323G>C , CM000684.2:g.42128323G>C	GRCh38
NC_000022.10:g.42524325G>C , CM000684.1:g.42524325G>C	GRCh37
NC_000022.9:g.40854269G>C	NCBI36
NG_008376.3:g.6669C>G
NG_008376.4:g.7488C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.541C>G	ENSP00000353241.6:p.His181Asp
ENST00000645361.2:c.694C>G MANE Select	ENSP00000496150.1:p.His232Asp
ENST00000359033.4:c.541C>G	ENSP00000351927.4:p.His181Asp
ENST00000360124.9:c.361C>G	ENSP00000353241.5:p.His121Asp
ENST00000360608.9:c.694C>G	ENSP00000353820.5:p.His232Asp
ENST00000389970.7:c.628C>G	ENSP00000374620.4:p.His210Asp
ENST00000488442.1:n.1418C>G
NM_000106.5:c.694C>G	NP_000097.3:p.His232Asp
NM_001025161.2:c.541C>G	NP_001020332.2:p.His181Asp
XM_011529966.1:c.694C>G	XP_011528268.1:p.His232Asp
XM_011529967.1:c.694C>G	XP_011528269.1:p.His232Asp
XM_011529968.1:c.694C>G	XP_011528270.1:p.His232Asp
XM_011529969.1:c.550C>G	XP_011528271.1:p.His184Asp
XM_011529970.1:c.541C>G	XP_011528272.1:p.His181Asp
XM_011529971.1:c.550C>G	XP_011528273.1:p.His184Asp
XM_011529972.1:c.694C>G	XP_011528274.1:p.His232Asp
NM_000106.6:c.694C>G MANE Select	NP_000097.3:p.His232Asp
NM_001025161.3:c.541C>G	NP_001020332.2:p.His181Asp