Canonical Allele Identifier: CA324664331

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1052632496
• gnomAD v3: 22-42126521-T-C
• gnomAD v4: 22-42126521-T-C
• MyVariant Identifiers: chr22:g.42522523T>C (hg19) ; chr22:g.42126521T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126521T>C , CM000684.2:g.42126521T>C	GRCh38
NC_000022.10:g.42522523T>C , CM000684.1:g.42522523T>C	GRCh37
NC_000022.9:g.40852467T>C	NCBI36
NG_008376.3:g.8471A>G
NG_008376.4:g.9290A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1345A>G	ENSP00000353241.6:n.1345A>G
ENST00000645361.2:c.*53A>G MANE Select	ENSP00000496150.1:n.*53A>G
ENST00000360124.9:c.1165A>G	ENSP00000353241.5:n.1165A>G
ENST00000360608.9:c.*53A>G	ENSP00000353820.5:n.*53A>G
ENST00000389970.7:c.*53A>G	ENSP00000374620.4:n.*53A>G
NM_000106.5:c.*53A>G	NP_000097.3:n.*53A>G
NM_001025161.2:c.*53A>G	NP_001020332.2:n.*53A>G
XM_011529966.1:c.1452+95A>G	XP_011528268.1:n.1452+95A>G
XM_011529967.1:c.1452+95A>G	XP_011528269.1:n.1452+95A>G
XM_011529968.1:c.1452+95A>G	XP_011528270.1:n.1452+95A>G
XM_011529969.1:c.1308+95A>G	XP_011528271.1:n.1308+95A>G
XM_011529970.1:c.1299+95A>G	XP_011528272.1:n.1299+95A>G
XM_011529971.1:c.*53A>G	XP_011528273.1:n.*53A>G
NM_000106.6:c.*53A>G MANE Select	NP_000097.3:n.*53A>G
NM_001025161.3:c.*53A>G	NP_001020332.2:n.*53A>G