Canonical Allele Identifier: CA514705938
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1932571313
gnomAD v4: 22-42132647-A-G
MyVariant Identifiers: chr22:g.42528654A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132647A>G , CM000684.2:g.42132647A>G GRCh38
NC_000022.10:g.42528654A>G , CM000684.1:g.42528654A>G GRCh37
NC_000022.9:g.40858598A>G NCBI36
NG_008376.3:g.2345T>C
NG_008376.4:g.3164T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.105A>G
XM_011529967.1:c.-1045-811T>C XP_011528269.1:n.-1045-811T>C
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