Canonical Allele Identifier: CA2406577760

Gene: CYP2D6

Linked Data

• dbSNP Id: rs892629477
• gnomAD v4: 22-42126527-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126527A>G , CM000684.2:g.42126527A>G	GRCh38
NC_000022.10:g.42522529A>G , CM000684.1:g.42522529A>G	GRCh37
NC_000022.9:g.40852473A>G	NCBI36
NG_008376.3:g.8465T>C
NG_008376.4:g.9284T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1339T>C	ENSP00000353241.6:n.1339T>C
ENST00000645361.2:c.*47T>C MANE Select	ENSP00000496150.1:n.*47T>C
ENST00000360124.9:c.1159T>C	ENSP00000353241.5:n.1159T>C
ENST00000360608.9:c.*47T>C	ENSP00000353820.5:n.*47T>C
ENST00000389970.7:c.*47T>C	ENSP00000374620.4:n.*47T>C
NM_000106.5:c.*47T>C	NP_000097.3:n.*47T>C
NM_001025161.2:c.*47T>C	NP_001020332.2:n.*47T>C
XM_011529966.1:c.1452+89T>C	XP_011528268.1:n.1452+89T>C
XM_011529967.1:c.1452+89T>C	XP_011528269.1:n.1452+89T>C
XM_011529968.1:c.1452+89T>C	XP_011528270.1:n.1452+89T>C
XM_011529969.1:c.1308+89T>C	XP_011528271.1:n.1308+89T>C
XM_011529970.1:c.1299+89T>C	XP_011528272.1:n.1299+89T>C
XM_011529971.1:c.*47T>C	XP_011528273.1:n.*47T>C
NM_000106.6:c.*47T>C MANE Select	NP_000097.3:n.*47T>C
NM_001025161.3:c.*47T>C	NP_001020332.2:n.*47T>C