Canonical Allele Identifier: CA753332059

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1216121743
• gnomAD v3: 22-42130906-T-C
• gnomAD v4: 22-42130906-T-C
• MyVariant Identifiers: chr22:g.42130906T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130906T>C , CM000684.2:g.42130906T>C	GRCh38
NC_000022.10:g.42526908T>C , CM000684.1:g.42526908T>C	GRCh37
NC_000022.9:g.40856852T>C	NCBI36
NG_008376.3:g.4086A>G
NG_008376.4:g.4905A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360608.9:c.-115A>G	ENSP00000353820.5:n.-115A>G
XM_011529966.1:c.-115A>G	XP_011528268.1:n.-115A>G
XM_011529967.1:c.-115A>G	XP_011528269.1:n.-115A>G
XM_011529968.1:c.-115A>G	XP_011528270.1:n.-115A>G
XM_011529969.1:c.37+391A>G	XP_011528271.1:n.37+391A>G
XM_011529970.1:c.-115A>G	XP_011528272.1:n.-115A>G
XM_011529971.1:c.37+391A>G	XP_011528273.1:n.37+391A>G
XM_011529972.1:c.-115A>G	XP_011528274.1:n.-115A>G
XR_430455.2:n.328+218T>C
XR_002958749.1:n.275+218T>C