Canonical Allele Identifier: CA324677598

Gene: CYP2D6

Linked Data

• dbSNP Id: rs900255625
• gnomAD v3: 22-42132735-C-T
• gnomAD v4: 22-42132735-C-T
• MyVariant Identifiers: chr22:g.42528742C>T (hg19) ; chr22:g.42132735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42132735C>T , CM000684.2:g.42132735C>T	GRCh38
NC_000022.10:g.42528742C>T , CM000684.1:g.42528742C>T	GRCh37
NC_000022.9:g.40858686C>T	NCBI36
NG_008376.3:g.2257G>A
NG_008376.4:g.3076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417586.1:n.193C>T
XM_011529967.1:c.-1045-899G>A	XP_011528269.1:n.-1045-899G>A