Canonical Allele Identifier: CA514799837

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522615C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126613C>G , CM000684.2:g.42126613C>G	GRCh38
NC_000022.10:g.42522615C>G , CM000684.1:g.42522615C>G	GRCh37
NC_000022.9:g.40852559C>G	NCBI36
NG_008376.3:g.8379G>C
NG_008376.4:g.9198G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1253G>C	ENSP00000353241.6:n.1253G>C
ENST00000645361.2:c.1455G>C MANE Select	ENSP00000496150.1:p.Val485=
ENST00000359033.4:c.1302G>C	ENSP00000351927.4:p.Val434=
ENST00000360124.9:c.1073G>C	ENSP00000353241.5:n.1073G>C
ENST00000360608.9:c.1455G>C	ENSP00000353820.5:p.Val485=
ENST00000389970.7:c.1446G>C	ENSP00000374620.4:p.Val482=
ENST00000488442.1:n.2179G>C
NM_000106.5:c.1455G>C	NP_000097.3:p.Val485=
NM_001025161.2:c.1302G>C	NP_001020332.2:p.Val434=
XM_011529966.1:c.1452+3G>C	XP_011528268.1:n.1452+3G>C
XM_011529967.1:c.1452+3G>C	XP_011528269.1:n.1452+3G>C
XM_011529968.1:c.1452+3G>C	XP_011528270.1:n.1452+3G>C
XM_011529969.1:c.1308+3G>C	XP_011528271.1:n.1308+3G>C
XM_011529970.1:c.1299+3G>C	XP_011528272.1:n.1299+3G>C
XM_011529971.1:c.1311G>C	XP_011528273.1:p.Val437=
NM_000106.6:c.1455G>C MANE Select	NP_000097.3:p.Val485=
NM_001025161.3:c.1302G>C	NP_001020332.2:p.Val434=