Canonical Allele Identifier: CA514706521
Gene: CYP2D6 HGNC NCBI

Linked Data

gnomAD v4: 22-42132746-T-C
MyVariant Identifiers: chr22:g.42528753T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132746T>C , CM000684.2:g.42132746T>C GRCh38
NC_000022.10:g.42528753T>C , CM000684.1:g.42528753T>C GRCh37
NC_000022.9:g.40858697T>C NCBI36
NG_008376.3:g.2246A>G
NG_008376.4:g.3065A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.204T>C
XM_011529967.1:c.-1045-910A>G XP_011528269.1:n.-1045-910A>G
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