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Canonical Allele Identifier:
CA753333138
Gene: CYP2D6
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.42132375G>A
Linked Data - Sequence & Population
gnomAD v3:
22:42132375 G / A
gnomAD v4:
chr22-42132375-G-A
Joint Max Group AF
0.0000049 (NFE)
Genomes Max Group AF
0.00000491 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1080985
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.42132375G>A , CM000684.2:g.42132375G>A
GRCh38
NG_008376.3:g.2617C>T
NG_008376.4:g.3436C>T
Transcript Alleles
HGVS
Amino-acid Change
XM_011529967.1:c.-1045-539C>T
XP_011528269.1:n.-1045-539C>T
Search 100 bp 5'
Search 100 bp 3'