Canonical Allele Identifier: CA639488964
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1159094561
gnomAD v2: 22-42527004-GCTGCTCCAGAGGTTCTTGCCCCTGCTTC-G
gnomAD v3: 22-42131002-GCTGCTCCAGAGGTTCTTGCCCCTGCTTC-G
gnomAD v4: 22-42131002-GCTGCTCCAGAGGTTCTTGCCCCTGCTTC-G
MyVariant Identifiers: chr22:g.42527005_42527032del (hg19) chr22:g.42131003_42131030del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131012_42131039del , CM000684.2:g.42131012_42131039del GRCh38
NC_000022.10:g.42527014_42527041del , CM000684.1:g.42527014_42527041del GRCh37
NC_000022.9:g.40856958_40856985del NCBI36
NG_008376.3:g.3962_3989del
NG_008376.4:g.4781_4808del

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-239_-212del XP_011528268.1:n.-239_-212del
XM_011529967.1:c.-239_-212del XP_011528269.1:n.-239_-212del
XM_011529968.1:c.-239_-212del XP_011528270.1:n.-239_-212del
XM_011529969.1:c.37+267_37+294del XP_011528271.1:n.37+267_37+294del
XM_011529970.1:c.-239_-212del XP_011528272.1:n.-239_-212del
XM_011529971.1:c.37+267_37+294del XP_011528273.1:n.37+267_37+294del
XM_011529972.1:c.-239_-212del XP_011528274.1:n.-239_-212del
XR_430455.2:n.328+324_328+351del
XR_002958749.1:n.275+324_275+351del
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