Canonical Allele Identifier: CA411772638

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523920G>C (hg19) ; chr22:g.42127918G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127918G>C , CM000684.2:g.42127918G>C	GRCh38
NC_000022.10:g.42523920G>C , CM000684.1:g.42523920G>C	GRCh37
NC_000022.9:g.40853864G>C	NCBI36
NG_008376.3:g.7074C>G
NG_008376.4:g.7893C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.707C>G	ENSP00000353241.6:p.Ser236Cys
ENST00000645361.2:c.909C>G MANE Select	ENSP00000496150.1:p.Phe303Leu
ENST00000359033.4:c.756C>G	ENSP00000351927.4:p.Phe252Leu
ENST00000360124.9:c.527C>G	ENSP00000353241.5:p.Ser176Cys
ENST00000360608.9:c.909C>G	ENSP00000353820.5:p.Phe303Leu
ENST00000389970.7:c.843C>G	ENSP00000374620.4:p.Phe281Leu
ENST00000488442.1:n.1633C>G
NM_000106.5:c.909C>G	NP_000097.3:p.Phe303Leu
NM_001025161.2:c.756C>G	NP_001020332.2:p.Phe252Leu
XM_011529966.1:c.909C>G	XP_011528268.1:p.Phe303Leu
XM_011529967.1:c.909C>G	XP_011528269.1:p.Phe303Leu
XM_011529968.1:c.909C>G	XP_011528270.1:p.Phe303Leu
XM_011529969.1:c.765C>G	XP_011528271.1:p.Phe255Leu
XM_011529970.1:c.756C>G	XP_011528272.1:p.Phe252Leu
XM_011529971.1:c.765C>G	XP_011528273.1:p.Phe255Leu
XM_011529972.1:c.843+256C>G	XP_011528274.1:n.843+256C>G
NM_000106.6:c.909C>G MANE Select	NP_000097.3:p.Phe303Leu
NM_001025161.3:c.756C>G	NP_001020332.2:p.Phe252Leu