Canonical Allele Identifier: CA514800548

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126658-A-C
• MyVariant Identifiers: chr22:g.42522660A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126658A>C , CM000684.2:g.42126658A>C	GRCh38
NC_000022.10:g.42522660A>C , CM000684.1:g.42522660A>C	GRCh37
NC_000022.9:g.40852604A>C	NCBI36
NG_008376.3:g.8334T>G
NG_008376.4:g.9153T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1208T>G	ENSP00000353241.6:n.1208T>G
ENST00000645361.2:c.1410T>G MANE Select	ENSP00000496150.1:p.Thr470=
ENST00000359033.4:c.1257T>G	ENSP00000351927.4:p.Thr419=
ENST00000360124.9:c.1028T>G	ENSP00000353241.5:n.1028T>G
ENST00000360608.9:c.1410T>G	ENSP00000353820.5:p.Thr470=
ENST00000389970.7:c.1401T>G	ENSP00000374620.4:p.Thr467=
ENST00000488442.1:n.2134T>G
NM_000106.5:c.1410T>G	NP_000097.3:p.Thr470=
NM_001025161.2:c.1257T>G	NP_001020332.2:p.Thr419=
XM_011529966.1:c.1410T>G	XP_011528268.1:p.Thr470=
XM_011529967.1:c.1410T>G	XP_011528269.1:p.Thr470=
XM_011529968.1:c.1410T>G	XP_011528270.1:p.Thr470=
XM_011529969.1:c.1266T>G	XP_011528271.1:p.Thr422=
XM_011529970.1:c.1257T>G	XP_011528272.1:p.Thr419=
XM_011529971.1:c.1266T>G	XP_011528273.1:p.Thr422=
NM_000106.6:c.1410T>G MANE Select	NP_000097.3:p.Thr470=
NM_001025161.3:c.1257T>G	NP_001020332.2:p.Thr419=