Canonical Allele Identifier: CA639827876

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1199132762
• gnomAD v2: 22-42522548-G-A
• gnomAD v4: 22-42126546-G-A
• MyVariant Identifiers: chr22:g.42522548G>A (hg19) ; chr22:g.42126546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126546G>A , CM000684.2:g.42126546G>A	GRCh38
NC_000022.10:g.42522548G>A , CM000684.1:g.42522548G>A	GRCh37
NC_000022.9:g.40852492G>A	NCBI36
NG_008376.3:g.8446C>T
NG_008376.4:g.9265C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1320C>T	ENSP00000353241.6:n.1320C>T
ENST00000645361.2:c.*28C>T MANE Select	ENSP00000496150.1:n.*28C>T
ENST00000360124.9:c.1140C>T	ENSP00000353241.5:n.1140C>T
ENST00000360608.9:c.*28C>T	ENSP00000353820.5:n.*28C>T
ENST00000389970.7:c.*28C>T	ENSP00000374620.4:n.*28C>T
ENST00000488442.1:n.2246C>T
NM_000106.5:c.*28C>T	NP_000097.3:n.*28C>T
NM_001025161.2:c.*28C>T	NP_001020332.2:n.*28C>T
XM_011529966.1:c.1452+70C>T	XP_011528268.1:n.1452+70C>T
XM_011529967.1:c.1452+70C>T	XP_011528269.1:n.1452+70C>T
XM_011529968.1:c.1452+70C>T	XP_011528270.1:n.1452+70C>T
XM_011529969.1:c.1308+70C>T	XP_011528271.1:n.1308+70C>T
XM_011529970.1:c.1299+70C>T	XP_011528272.1:n.1299+70C>T
XM_011529971.1:c.*28C>T	XP_011528273.1:n.*28C>T
NM_000106.6:c.*28C>T MANE Select	NP_000097.3:n.*28C>T
NM_001025161.3:c.*28C>T	NP_001020332.2:n.*28C>T