Canonical Allele Identifier: CA514706201

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1374106155
• MyVariant Identifiers: chr22:g.42528700G>C (hg19) ; chr22:g.42132693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42132693G>C , CM000684.2:g.42132693G>C	GRCh38
NC_000022.10:g.42528700G>C , CM000684.1:g.42528700G>C	GRCh37
NC_000022.9:g.40858644G>C	NCBI36
NG_008376.3:g.2299C>G
NG_008376.4:g.3118C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417586.1:n.151G>C
XM_011529967.1:c.-1045-857C>G	XP_011528269.1:n.-1045-857C>G