Canonical Allele Identifier: CA10265191

Gene: CYP2D6

Linked Data

• dbSNP Id: rs373668214
• ExAC: 22:42525230 A / G
• gnomAD v2: 22-42525230-A-G
• gnomAD v3: 22-42129228-A-G
• gnomAD v4: 22-42129228-A-G
• MyVariant Identifiers: chr22:g.42525230A>G (hg19) ; chr22:g.42129228A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129228A>G , CM000684.2:g.42129228A>G	GRCh38
NC_000022.10:g.42525230A>G , CM000684.1:g.42525230A>G	GRCh37
NC_000022.9:g.40855174A>G	NCBI36
NG_008376.3:g.5764T>C
NG_008376.4:g.6583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-284T>C	ENSP00000353241.6:n.353-284T>C
ENST00000645361.2:c.353-43T>C MANE Select	ENSP00000496150.1:n.353-43T>C
ENST00000359033.4:c.353-284T>C	ENSP00000351927.4:n.353-284T>C
ENST00000360124.9:c.173-284T>C	ENSP00000353241.5:n.173-284T>C
ENST00000360608.9:c.353-43T>C	ENSP00000353820.5:n.353-43T>C
ENST00000389970.7:c.287-43T>C	ENSP00000374620.4:n.287-43T>C
ENST00000488442.1:n.1077-43T>C
NM_000106.5:c.353-43T>C	NP_000097.3:n.353-43T>C
NM_001025161.2:c.353-284T>C	NP_001020332.2:n.353-284T>C
XM_011529966.1:c.353-43T>C	XP_011528268.1:n.353-43T>C
XM_011529967.1:c.353-43T>C	XP_011528269.1:n.353-43T>C
XM_011529968.1:c.353-43T>C	XP_011528270.1:n.353-43T>C
XM_011529969.1:c.210-43T>C	XP_011528271.1:n.210-43T>C
XM_011529970.1:c.353-284T>C	XP_011528272.1:n.353-284T>C
XM_011529971.1:c.210-43T>C	XP_011528273.1:n.210-43T>C
XM_011529972.1:c.353-43T>C	XP_011528274.1:n.353-43T>C
NM_000106.6:c.353-43T>C MANE Select	NP_000097.3:n.353-43T>C
NM_001025161.3:c.353-284T>C	NP_001020332.2:n.353-284T>C