Canonical Allele Identifier: CA324664507

Gene: CYP2D6

Linked Data

• dbSNP Id: rs74478221
• MyVariant Identifiers: chr22:g.42522626C>T (hg19) ; chr22:g.42126624C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126624C>T , CM000684.2:g.42126624C>T	GRCh38
NC_000022.10:g.42522626C>T , CM000684.1:g.42522626C>T	GRCh37
NC_000022.9:g.40852570C>T	NCBI36
NG_008376.3:g.8368G>A
NG_008376.4:g.9187G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1242G>A	ENSP00000353241.6:n.1242G>A
ENST00000645361.2:c.1444G>A MANE Select	ENSP00000496150.1:p.Ala482Thr
ENST00000359033.4:c.1291G>A	ENSP00000351927.4:p.Ala431Thr
ENST00000360124.9:c.1062G>A	ENSP00000353241.5:n.1062G>A
ENST00000360608.9:c.1444G>A	ENSP00000353820.5:p.Ala482Thr
ENST00000389970.7:c.1435G>A	ENSP00000374620.4:p.Ala479Thr
ENST00000488442.1:n.2168G>A
NM_000106.5:c.1444G>A	NP_000097.3:p.Ala482Thr
NM_001025161.2:c.1291G>A	NP_001020332.2:p.Ala431Thr
XM_011529966.1:c.1444G>A	XP_011528268.1:p.Ala482Thr
XM_011529967.1:c.1444G>A	XP_011528269.1:p.Ala482Thr
XM_011529968.1:c.1444G>A	XP_011528270.1:p.Ala482Thr
XM_011529969.1:c.1300G>A	XP_011528271.1:p.Ala434Thr
XM_011529970.1:c.1291G>A	XP_011528272.1:p.Ala431Thr
XM_011529971.1:c.1300G>A	XP_011528273.1:p.Ala434Thr
NM_000106.6:c.1444G>A MANE Select	NP_000097.3:p.Ala482Thr
NM_001025161.3:c.1291G>A	NP_001020332.2:p.Ala431Thr