Canonical Allele Identifier: CA411772570

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1180181277
• MyVariant Identifiers: chr22:g.42523903G>C (hg19) ; chr22:g.42127901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127901G>C , CM000684.2:g.42127901G>C	GRCh38
NC_000022.10:g.42523903G>C , CM000684.1:g.42523903G>C	GRCh37
NC_000022.9:g.40853847G>C	NCBI36
NG_008376.3:g.7091C>G
NG_008376.4:g.7910C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.724C>G	ENSP00000353241.6:n.724C>G
ENST00000645361.2:c.926C>G MANE Select	ENSP00000496150.1:p.Thr309Ser
ENST00000359033.4:c.773C>G	ENSP00000351927.4:p.Thr258Ser
ENST00000360124.9:c.544C>G	ENSP00000353241.5:n.544C>G
ENST00000360608.9:c.926C>G	ENSP00000353820.5:p.Thr309Ser
ENST00000389970.7:c.860C>G	ENSP00000374620.4:p.Thr287Ser
ENST00000488442.1:n.1650C>G
NM_000106.5:c.926C>G	NP_000097.3:p.Thr309Ser
NM_001025161.2:c.773C>G	NP_001020332.2:p.Thr258Ser
XM_011529966.1:c.926C>G	XP_011528268.1:p.Thr309Ser
XM_011529967.1:c.926C>G	XP_011528269.1:p.Thr309Ser
XM_011529968.1:c.926C>G	XP_011528270.1:p.Thr309Ser
XM_011529969.1:c.782C>G	XP_011528271.1:p.Thr261Ser
XM_011529970.1:c.773C>G	XP_011528272.1:p.Thr258Ser
XM_011529971.1:c.782C>G	XP_011528273.1:p.Thr261Ser
XM_011529972.1:c.844-267C>G	XP_011528274.1:n.844-267C>G
NM_000106.6:c.926C>G MANE Select	NP_000097.3:p.Thr309Ser
NM_001025161.3:c.773C>G	NP_001020332.2:p.Thr258Ser