Canonical Allele Identifier: CA10264965

Gene: CYP2D6

Linked Data

• dbSNP Id: rs780522166
• ExAC: 22:42524764 T / C
• gnomAD v2: 22-42524764-T-C
• gnomAD v3: 22-42128762-T-C
• gnomAD v4: 22-42128762-T-C
• MyVariant Identifiers: chr22:g.42524764T>C (hg19) ; chr22:g.42128762T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128762T>C , CM000684.2:g.42128762T>C	GRCh38
NC_000022.10:g.42524764T>C , CM000684.1:g.42524764T>C	GRCh37
NC_000022.9:g.40854708T>C	NCBI36
NG_008376.3:g.6230A>G
NG_008376.4:g.7049A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.513+22A>G	ENSP00000353241.6:n.513+22A>G
ENST00000645361.2:c.666+22A>G MANE Select	ENSP00000496150.1:n.666+22A>G
ENST00000359033.4:c.513+22A>G	ENSP00000351927.4:n.513+22A>G
ENST00000360124.9:c.333+22A>G	ENSP00000353241.5:n.333+22A>G
ENST00000360608.9:c.666+22A>G	ENSP00000353820.5:n.666+22A>G
ENST00000389970.7:c.600+22A>G	ENSP00000374620.4:n.600+22A>G
ENST00000488442.1:n.1390+22A>G
NM_000106.5:c.666+22A>G	NP_000097.3:n.666+22A>G
NM_001025161.2:c.513+22A>G	NP_001020332.2:n.513+22A>G
XM_011529966.1:c.666+22A>G	XP_011528268.1:n.666+22A>G
XM_011529967.1:c.666+22A>G	XP_011528269.1:n.666+22A>G
XM_011529968.1:c.666+22A>G	XP_011528270.1:n.666+22A>G
XM_011529969.1:c.522+22A>G	XP_011528271.1:n.522+22A>G
XM_011529970.1:c.513+22A>G	XP_011528272.1:n.513+22A>G
XM_011529971.1:c.522+22A>G	XP_011528273.1:n.522+22A>G
XM_011529972.1:c.666+22A>G	XP_011528274.1:n.666+22A>G
NM_000106.6:c.666+22A>G MANE Select	NP_000097.3:n.666+22A>G
NM_001025161.3:c.513+22A>G	NP_001020332.2:n.513+22A>G