Canonical Allele Identifier: CA411771436

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42127496-G-C
• MyVariant Identifiers: chr22:g.42523498G>C (hg19) ; chr22:g.42127496G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127496G>C , CM000684.2:g.42127496G>C	GRCh38
NC_000022.10:g.42523498G>C , CM000684.1:g.42523498G>C	GRCh37
NC_000022.9:g.40853442G>C	NCBI36
NG_008376.3:g.7496C>G
NG_008376.4:g.8315C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.922C>G	ENSP00000353241.6:n.922C>G
ENST00000645361.2:c.1124C>G MANE Select	ENSP00000496150.1:p.Thr375Ser
ENST00000359033.4:c.971C>G	ENSP00000351927.4:p.Thr324Ser
ENST00000360124.9:c.742C>G	ENSP00000353241.5:n.742C>G
ENST00000360608.9:c.1124C>G	ENSP00000353820.5:p.Thr375Ser
ENST00000389970.7:c.1115C>G	ENSP00000374620.4:p.Thr372Ser
ENST00000488442.1:n.1848C>G
NM_000106.5:c.1124C>G	NP_000097.3:p.Thr375Ser
NM_001025161.2:c.971C>G	NP_001020332.2:p.Thr324Ser
XM_011529966.1:c.1124C>G	XP_011528268.1:p.Thr375Ser
XM_011529967.1:c.1124C>G	XP_011528269.1:p.Thr375Ser
XM_011529968.1:c.1124C>G	XP_011528270.1:p.Thr375Ser
XM_011529969.1:c.980C>G	XP_011528271.1:p.Thr327Ser
XM_011529970.1:c.971C>G	XP_011528272.1:p.Thr324Ser
XM_011529971.1:c.980C>G	XP_011528273.1:p.Thr327Ser
NM_000106.6:c.1124C>G MANE Select	NP_000097.3:p.Thr375Ser
NM_001025161.3:c.971C>G	NP_001020332.2:p.Thr324Ser