Canonical Allele Identifier: CA324675775
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs28371694
MyVariant Identifiers: chr22:g.42526890_42526891insA (hg19) chr22:g.42130888_42130889insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130888_42130889insA , CM000684.2:g.42130888_42130889insA GRCh38
NC_000022.10:g.42526890_42526891insA , CM000684.1:g.42526890_42526891insA GRCh37
NC_000022.9:g.40856834_40856835insA NCBI36
NG_008376.3:g.4103_4104insT
NG_008376.4:g.4922_4923insT

Transcript Alleles

HGVS Amino-acid change
ENST00000360608.9:c.-98_-97insT ENSP00000353820.5:n.-98_-97insT
XM_011529966.1:c.-98_-97insT XP_011528268.1:n.-98_-97insT
XM_011529967.1:c.-98_-97insT XP_011528269.1:n.-98_-97insT
XM_011529968.1:c.-98_-97insT XP_011528270.1:n.-98_-97insT
XM_011529969.1:c.37+408_37+409insT XP_011528271.1:n.37+408_37+409insT
XM_011529970.1:c.-98_-97insT XP_011528272.1:n.-98_-97insT
XM_011529971.1:c.37+408_37+409insT XP_011528273.1:n.37+408_37+409insT
XM_011529972.1:c.-98_-97insT XP_011528274.1:n.-98_-97insT
XR_430455.2:n.328+200_328+201insA
XR_002958749.1:n.275+200_275+201insA
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