Canonical Allele Identifier: CA324663922
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs927827798
gnomAD v3: 22-42126064-C-G
gnomAD v4: 22-42126064-C-G
MyVariant Identifiers: chr22:g.42522069C>G (hg19) chr22:g.42126064C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126064C>G , CM000684.2:g.42126064C>G GRCh38
NC_000022.10:g.42522069C>G , CM000684.1:g.42522069C>G GRCh37
NC_000022.9:g.40852013C>G NCBI36
NG_008376.3:g.8928G>C
NG_008376.4:g.9747G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-111G>C XP_011528268.1:n.1453-111G>C
XM_011529967.1:c.1453-111G>C XP_011528269.1:n.1453-111G>C
XM_011529968.1:c.1453-137G>C XP_011528270.1:n.1453-137G>C
XM_011529969.1:c.1309-111G>C XP_011528271.1:n.1309-111G>C
XM_011529970.1:c.1300-111G>C XP_011528272.1:n.1300-111G>C
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