Canonical Allele Identifier: CA411773967

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128877-G-T
• MyVariant Identifiers: chr22:g.42524879G>T (hg19) ; chr22:g.42128877G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128877G>T , CM000684.2:g.42128877G>T	GRCh38
NC_000022.10:g.42524879G>T , CM000684.1:g.42524879G>T	GRCh37
NC_000022.9:g.40854823G>T	NCBI36
NG_008376.3:g.6115C>A
NG_008376.4:g.6934C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.420C>A	ENSP00000353241.6:p.Cys140Ter
ENST00000645361.2:c.573C>A MANE Select	ENSP00000496150.1:p.Cys191Ter
ENST00000359033.4:c.420C>A	ENSP00000351927.4:p.Cys140Ter
ENST00000360124.9:c.240C>A	ENSP00000353241.5:p.Cys80Ter
ENST00000360608.9:c.573C>A	ENSP00000353820.5:p.Cys191Ter
ENST00000389970.7:c.507C>A	ENSP00000374620.4:p.Cys169Ter
ENST00000488442.1:n.1297C>A
NM_000106.5:c.573C>A	NP_000097.3:p.Cys191Ter
NM_001025161.2:c.420C>A	NP_001020332.2:p.Cys140Ter
XM_011529966.1:c.573C>A	XP_011528268.1:p.Cys191Ter
XM_011529967.1:c.573C>A	XP_011528269.1:p.Cys191Ter
XM_011529968.1:c.573C>A	XP_011528270.1:p.Cys191Ter
XM_011529969.1:c.429C>A	XP_011528271.1:p.Cys143Ter
XM_011529970.1:c.420C>A	XP_011528272.1:p.Cys140Ter
XM_011529971.1:c.429C>A	XP_011528273.1:p.Cys143Ter
XM_011529972.1:c.573C>A	XP_011528274.1:p.Cys191Ter
NM_000106.6:c.573C>A MANE Select	NP_000097.3:p.Cys191Ter
NM_001025161.3:c.420C>A	NP_001020332.2:p.Cys140Ter