Canonical Allele Identifier: CA514800256

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523977C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127975C>G , CM000684.2:g.42127975C>G	GRCh38
NC_000022.10:g.42523977C>G , CM000684.1:g.42523977C>G	GRCh37
NC_000022.9:g.40853921C>G	NCBI36
NG_008376.3:g.7017G>C
NG_008376.4:g.7836G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.691-41G>C	ENSP00000353241.6:n.691-41G>C
ENST00000645361.2:c.852G>C MANE Select	ENSP00000496150.1:p.Gly284=
ENST00000359033.4:c.699G>C	ENSP00000351927.4:p.Gly233=
ENST00000360124.9:c.511-41G>C	ENSP00000353241.5:n.511-41G>C
ENST00000360608.9:c.852G>C	ENSP00000353820.5:p.Gly284=
ENST00000389970.7:c.786G>C	ENSP00000374620.4:p.Gly262=
ENST00000488442.1:n.1576G>C
NM_000106.5:c.852G>C	NP_000097.3:p.Gly284=
NM_001025161.2:c.699G>C	NP_001020332.2:p.Gly233=
XM_011529966.1:c.852G>C	XP_011528268.1:p.Gly284=
XM_011529967.1:c.852G>C	XP_011528269.1:p.Gly284=
XM_011529968.1:c.852G>C	XP_011528270.1:p.Gly284=
XM_011529969.1:c.708G>C	XP_011528271.1:p.Gly236=
XM_011529970.1:c.699G>C	XP_011528272.1:p.Gly233=
XM_011529971.1:c.708G>C	XP_011528273.1:p.Gly236=
XM_011529972.1:c.843+199G>C	XP_011528274.1:n.843+199G>C
NM_000106.6:c.852G>C MANE Select	NP_000097.3:p.Gly284=
NM_001025161.3:c.699G>C	NP_001020332.2:p.Gly233=