Canonical Allele Identifier: CA639488972

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1231093114
• gnomAD v2: 22-42527102-C-T
• MyVariant Identifiers: chr22:g.42527102C>T (hg19) ; chr22:g.42131100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42131100C>T , CM000684.2:g.42131100C>T	GRCh38
NC_000022.10:g.42527102C>T , CM000684.1:g.42527102C>T	GRCh37
NC_000022.9:g.40857046C>T	NCBI36
NG_008376.3:g.3892G>A
NG_008376.4:g.4711G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.-309G>A	XP_011528268.1:n.-309G>A
XM_011529967.1:c.-309G>A	XP_011528269.1:n.-309G>A
XM_011529968.1:c.-309G>A	XP_011528270.1:n.-309G>A
XM_011529969.1:c.37+197G>A	XP_011528271.1:n.37+197G>A
XM_011529970.1:c.-309G>A	XP_011528272.1:n.-309G>A
XM_011529971.1:c.37+197G>A	XP_011528273.1:n.37+197G>A
XM_011529972.1:c.-309G>A	XP_011528274.1:n.-309G>A
XR_430455.2:n.328+412C>T
XR_002958749.1:n.275+412C>T