Canonical Allele Identifier: CA324677591
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs966561152
gnomAD v2: 22-42528740-T-C
gnomAD v3: 22-42132733-T-C
gnomAD v4: 22-42132733-T-C
MyVariant Identifiers: chr22:g.42528740T>C (hg19) chr22:g.42132733T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132733T>C , CM000684.2:g.42132733T>C GRCh38
NC_000022.10:g.42528740T>C , CM000684.1:g.42528740T>C GRCh37
NC_000022.9:g.40858684T>C NCBI36
NG_008376.3:g.2259A>G
NG_008376.4:g.3078A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.191T>C
XM_011529967.1:c.-1045-897A>G XP_011528269.1:n.-1045-897A>G
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