Canonical Allele Identifier: CA514706757
Gene: CYP2D6 HGNC NCBI

Linked Data

gnomAD v4: 22-42132784-T-C
MyVariant Identifiers: chr22:g.42528791T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132784T>C , CM000684.2:g.42132784T>C GRCh38
NC_000022.10:g.42528791T>C , CM000684.1:g.42528791T>C GRCh37
NC_000022.9:g.40858735T>C NCBI36
NG_008376.3:g.2208A>G
NG_008376.4:g.3027A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.242T>C
XM_011529967.1:c.-1045-948A>G XP_011528269.1:n.-1045-948A>G
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