Canonical Allele Identifier: CA324676144

Gene: CYP2D6

Linked Data

• ClinVar Variation Id: 828823
• ClinVar RCV Id: RCV001028734
• dbSNP Id: rs530422334
• gnomAD v2: 22-42527147-T-C
• gnomAD v3: 22-42131145-T-C
• gnomAD v4: 22-42131145-T-C
• MyVariant Identifiers: chr22:g.42527147T>C (hg19) ; chr22:g.42131145T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42131145T>C , CM000684.2:g.42131145T>C	GRCh38
NC_000022.10:g.42527147T>C , CM000684.1:g.42527147T>C	GRCh37
NC_000022.9:g.40857091T>C	NCBI36
NG_008376.3:g.3847A>G
NG_008376.4:g.4666A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.-354A>G	XP_011528268.1:n.-354A>G
XM_011529967.1:c.-354A>G	XP_011528269.1:n.-354A>G
XM_011529968.1:c.-354A>G	XP_011528270.1:n.-354A>G
XM_011529969.1:c.37+152A>G	XP_011528271.1:n.37+152A>G
XM_011529970.1:c.-354A>G	XP_011528272.1:n.-354A>G
XM_011529971.1:c.37+152A>G	XP_011528273.1:n.37+152A>G
XM_011529972.1:c.-354A>G	XP_011528274.1:n.-354A>G
XR_430455.2:n.328+457T>C
XR_002958749.1:n.275+457T>C