Canonical Allele Identifier: CA514799585

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522579G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126577G>C , CM000684.2:g.42126577G>C	GRCh38
NC_000022.10:g.42522579G>C , CM000684.1:g.42522579G>C	GRCh37
NC_000022.9:g.40852523G>C	NCBI36
NG_008376.3:g.8415C>G
NG_008376.4:g.9234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1289C>G	ENSP00000353241.6:n.1289C>G
ENST00000645361.2:c.1491C>G MANE Select	ENSP00000496150.1:p.Arg497=
ENST00000359033.4:c.1338C>G	ENSP00000351927.4:p.Arg446=
ENST00000360124.9:c.1109C>G	ENSP00000353241.5:n.1109C>G
ENST00000360608.9:c.1491C>G	ENSP00000353820.5:p.Arg497=
ENST00000389970.7:c.1482C>G	ENSP00000374620.4:p.Arg494=
ENST00000488442.1:n.2215C>G
NM_000106.5:c.1491C>G	NP_000097.3:p.Arg497=
NM_001025161.2:c.1338C>G	NP_001020332.2:p.Arg446=
XM_011529966.1:c.1452+39C>G	XP_011528268.1:n.1452+39C>G
XM_011529967.1:c.1452+39C>G	XP_011528269.1:n.1452+39C>G
XM_011529968.1:c.1452+39C>G	XP_011528270.1:n.1452+39C>G
XM_011529969.1:c.1308+39C>G	XP_011528271.1:n.1308+39C>G
XM_011529970.1:c.1299+39C>G	XP_011528272.1:n.1299+39C>G
XM_011529971.1:c.1347C>G	XP_011528273.1:p.Arg449=
NM_000106.6:c.1491C>G MANE Select	NP_000097.3:p.Arg497=
NM_001025161.3:c.1338C>G	NP_001020332.2:p.Arg446=