Canonical Allele Identifier: CA2657031330

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42127834-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127834G>A , CM000684.2:g.42127834G>A	GRCh38
NC_000022.10:g.42523836G>A , CM000684.1:g.42523836G>A	GRCh37
NC_000022.9:g.40853780G>A	NCBI36
NG_008376.3:g.7158C>T
NG_008376.4:g.7977C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+8C>T	ENSP00000353241.6:n.783+8C>T
ENST00000645361.2:c.985+8C>T MANE Select	ENSP00000496150.1:n.985+8C>T
ENST00000359033.4:c.832+8C>T	ENSP00000351927.4:n.832+8C>T
ENST00000360124.9:c.603+8C>T	ENSP00000353241.5:n.603+8C>T
ENST00000360608.9:c.985+8C>T	ENSP00000353820.5:n.985+8C>T
ENST00000389970.7:c.919+8C>T	ENSP00000374620.4:n.919+8C>T
ENST00000488442.1:n.1709+8C>T
NM_000106.5:c.985+8C>T	NP_000097.3:n.985+8C>T
NM_001025161.2:c.832+8C>T	NP_001020332.2:n.832+8C>T
XM_011529966.1:c.985+8C>T	XP_011528268.1:n.985+8C>T
XM_011529967.1:c.985+8C>T	XP_011528269.1:n.985+8C>T
XM_011529968.1:c.985+8C>T	XP_011528270.1:n.985+8C>T
XM_011529969.1:c.841+8C>T	XP_011528271.1:n.841+8C>T
XM_011529970.1:c.832+8C>T	XP_011528272.1:n.832+8C>T
XM_011529971.1:c.841+8C>T	XP_011528273.1:n.841+8C>T
XM_011529972.1:c.844-200C>T	XP_011528274.1:n.844-200C>T
NM_000106.6:c.985+8C>T MANE Select	NP_000097.3:n.985+8C>T
NM_001025161.3:c.832+8C>T	NP_001020332.2:n.832+8C>T