Canonical Allele Identifier: CA324677520
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs377492110
gnomAD v2: 22-42528681-C-T
gnomAD v3: 22-42132674-C-T
gnomAD v4: 22-42132674-C-T
MyVariant Identifiers: chr22:g.42528681C>T (hg19) chr22:g.42132674C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132674C>T , CM000684.2:g.42132674C>T GRCh38
NC_000022.10:g.42528681C>T , CM000684.1:g.42528681C>T GRCh37
NC_000022.9:g.40858625C>T NCBI36
NG_008376.3:g.2318G>A
NG_008376.4:g.3137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.132C>T
XM_011529967.1:c.-1045-838G>A XP_011528269.1:n.-1045-838G>A
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