Canonical Allele Identifier: CA324664047
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs371495760
gnomAD v3: 22-42126150-C-T
gnomAD v4: 22-42126150-C-T
MyVariant Identifiers: chr22:g.42522152C>T (hg19) chr22:g.42126150C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126150C>T , CM000684.2:g.42126150C>T GRCh38
NC_000022.10:g.42522152C>T , CM000684.1:g.42522152C>T GRCh37
NC_000022.9:g.40852096C>T NCBI36
NG_008376.3:g.8842G>A
NG_008376.4:g.9661G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-197G>A XP_011528268.1:n.1453-197G>A
XM_011529967.1:c.1453-197G>A XP_011528269.1:n.1453-197G>A
XM_011529968.1:c.1453-223G>A XP_011528270.1:n.1453-223G>A
XM_011529969.1:c.1309-197G>A XP_011528271.1:n.1309-197G>A
XM_011529970.1:c.1300-197G>A XP_011528272.1:n.1300-197G>A
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