Canonical Allele Identifier: CA514706250
Gene: CYP2D6 HGNC NCBI

Linked Data

gnomAD v4: 22-42132702-G-C
MyVariant Identifiers: chr22:g.42528709G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42132702G>C , CM000684.2:g.42132702G>C GRCh38
NC_000022.10:g.42528709G>C , CM000684.1:g.42528709G>C GRCh37
NC_000022.9:g.40858653G>C NCBI36
NG_008376.3:g.2290C>G
NG_008376.4:g.3109C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000417586.1:n.160G>C
XM_011529967.1:c.-1045-866C>G XP_011528269.1:n.-1045-866C>G
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