Canonical Allele Identifier: CA2657029110

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126537-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126537C>G , CM000684.2:g.42126537C>G	GRCh38
NC_000022.10:g.42522539C>G , CM000684.1:g.42522539C>G	GRCh37
NC_000022.9:g.40852483C>G	NCBI36
NG_008376.3:g.8455G>C
NG_008376.4:g.9274G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1329G>C	ENSP00000353241.6:n.1329G>C
ENST00000645361.2:c.*37G>C MANE Select	ENSP00000496150.1:n.*37G>C
ENST00000360124.9:c.1149G>C	ENSP00000353241.5:n.1149G>C
ENST00000360608.9:c.*37G>C	ENSP00000353820.5:n.*37G>C
ENST00000389970.7:c.*37G>C	ENSP00000374620.4:n.*37G>C
ENST00000488442.1:n.2255G>C
NM_000106.5:c.*37G>C	NP_000097.3:n.*37G>C
NM_001025161.2:c.*37G>C	NP_001020332.2:n.*37G>C
XM_011529966.1:c.1452+79G>C	XP_011528268.1:n.1452+79G>C
XM_011529967.1:c.1452+79G>C	XP_011528269.1:n.1452+79G>C
XM_011529968.1:c.1452+79G>C	XP_011528270.1:n.1452+79G>C
XM_011529969.1:c.1308+79G>C	XP_011528271.1:n.1308+79G>C
XM_011529970.1:c.1299+79G>C	XP_011528272.1:n.1299+79G>C
XM_011529971.1:c.*37G>C	XP_011528273.1:n.*37G>C
NM_000106.6:c.*37G>C MANE Select	NP_000097.3:n.*37G>C
NM_001025161.3:c.*37G>C	NP_001020332.2:n.*37G>C