Canonical Allele Identifier: CA411769835

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522623A>C (hg19) ; chr22:g.42126621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126621A>C , CM000684.2:g.42126621A>C	GRCh38
NC_000022.10:g.42522623A>C , CM000684.1:g.42522623A>C	GRCh37
NC_000022.9:g.40852567A>C	NCBI36
NG_008376.3:g.8371T>G
NG_008376.4:g.9190T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1245T>G	ENSP00000353241.6:n.1245T>G
ENST00000645361.2:c.1447T>G MANE Select	ENSP00000496150.1:p.Phe483Val
ENST00000359033.4:c.1294T>G	ENSP00000351927.4:p.Phe432Val
ENST00000360124.9:c.1065T>G	ENSP00000353241.5:n.1065T>G
ENST00000360608.9:c.1447T>G	ENSP00000353820.5:p.Phe483Val
ENST00000389970.7:c.1438T>G	ENSP00000374620.4:p.Phe480Val
ENST00000488442.1:n.2171T>G
NM_000106.5:c.1447T>G	NP_000097.3:p.Phe483Val
NM_001025161.2:c.1294T>G	NP_001020332.2:p.Phe432Val
XM_011529966.1:c.1447T>G	XP_011528268.1:p.Phe483Val
XM_011529967.1:c.1447T>G	XP_011528269.1:p.Phe483Val
XM_011529968.1:c.1447T>G	XP_011528270.1:p.Phe483Val
XM_011529969.1:c.1303T>G	XP_011528271.1:p.Phe435Val
XM_011529970.1:c.1294T>G	XP_011528272.1:p.Phe432Val
XM_011529971.1:c.1303T>G	XP_011528273.1:p.Phe435Val
NM_000106.6:c.1447T>G MANE Select	NP_000097.3:p.Phe483Val
NM_001025161.3:c.1294T>G	NP_001020332.2:p.Phe432Val