Canonical Allele Identifier: CA324663916
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs79347391
gnomAD v3: 22-42126023-G-A
gnomAD v4: 22-42126023-G-A
MyVariant Identifiers: chr22:g.42522028G>A (hg19) chr22:g.42126023G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126023G>A , CM000684.2:g.42126023G>A GRCh38
NC_000022.10:g.42522028G>A , CM000684.1:g.42522028G>A GRCh37
NC_000022.9:g.40851972G>A NCBI36
NG_008376.4:g.9788C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-70C>T XP_011528268.1:n.1453-70C>T
XM_011529967.1:c.1453-70C>T XP_011528269.1:n.1453-70C>T
XM_011529968.1:c.1453-96C>T XP_011528270.1:n.1453-96C>T
XM_011529969.1:c.1309-70C>T XP_011528271.1:n.1309-70C>T
XM_011529970.1:c.1300-70C>T XP_011528272.1:n.1300-70C>T
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