Canonical Allele Identifier: CA411772476

Gene: CYP2D6

Linked Data

• dbSNP Id: rs767483427
• MyVariant Identifiers: chr22:g.42523879C>G (hg19) ; chr22:g.42127877C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127877C>G , CM000684.2:g.42127877C>G	GRCh38
NC_000022.10:g.42523879C>G , CM000684.1:g.42523879C>G	GRCh37
NC_000022.9:g.40853823C>G	NCBI36
NG_008376.3:g.7115G>C
NG_008376.4:g.7934G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.748G>C	ENSP00000353241.6:n.748G>C
ENST00000645361.2:c.950G>C MANE Select	ENSP00000496150.1:p.Gly317Ala
ENST00000359033.4:c.797G>C	ENSP00000351927.4:p.Gly266Ala
ENST00000360124.9:c.568G>C	ENSP00000353241.5:n.568G>C
ENST00000360608.9:c.950G>C	ENSP00000353820.5:p.Gly317Ala
ENST00000389970.7:c.884G>C	ENSP00000374620.4:p.Gly295Ala
ENST00000488442.1:n.1674G>C
NM_000106.5:c.950G>C	NP_000097.3:p.Gly317Ala
NM_001025161.2:c.797G>C	NP_001020332.2:p.Gly266Ala
XM_011529966.1:c.950G>C	XP_011528268.1:p.Gly317Ala
XM_011529967.1:c.950G>C	XP_011528269.1:p.Gly317Ala
XM_011529968.1:c.950G>C	XP_011528270.1:p.Gly317Ala
XM_011529969.1:c.806G>C	XP_011528271.1:p.Gly269Ala
XM_011529970.1:c.797G>C	XP_011528272.1:p.Gly266Ala
XM_011529971.1:c.806G>C	XP_011528273.1:p.Gly269Ala
XM_011529972.1:c.844-243G>C	XP_011528274.1:n.844-243G>C
NM_000106.6:c.950G>C MANE Select	NP_000097.3:p.Gly317Ala
NM_001025161.3:c.797G>C	NP_001020332.2:p.Gly266Ala