Canonical Allele Identifier: CA639488966
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1296951387
gnomAD v2: 22-42527060-C-G
gnomAD v3: 22-42131058-C-G
gnomAD v4: 22-42131058-C-G
MyVariant Identifiers: chr22:g.42527060C>G (hg19) chr22:g.42131058C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131058C>G , CM000684.2:g.42131058C>G GRCh38
NC_000022.10:g.42527060C>G , CM000684.1:g.42527060C>G GRCh37
NC_000022.9:g.40857004C>G NCBI36
NG_008376.3:g.3934G>C
NG_008376.4:g.4753G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-267G>C XP_011528268.1:n.-267G>C
XM_011529967.1:c.-267G>C XP_011528269.1:n.-267G>C
XM_011529968.1:c.-267G>C XP_011528270.1:n.-267G>C
XM_011529969.1:c.37+239G>C XP_011528271.1:n.37+239G>C
XM_011529970.1:c.-267G>C XP_011528272.1:n.-267G>C
XM_011529971.1:c.37+239G>C XP_011528273.1:n.37+239G>C
XM_011529972.1:c.-267G>C XP_011528274.1:n.-267G>C
XR_430455.2:n.328+370C>G
XR_002958749.1:n.275+370C>G
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