Canonical Allele Identifier: CA639488970
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1312232062
gnomAD v2: 22-42527069-G-A
gnomAD v3: 22-42131067-G-A
gnomAD v4: 22-42131067-G-A
MyVariant Identifiers: chr22:g.42527069G>A (hg19) chr22:g.42131067G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131067G>A , CM000684.2:g.42131067G>A GRCh38
NC_000022.10:g.42527069G>A , CM000684.1:g.42527069G>A GRCh37
NC_000022.9:g.40857013G>A NCBI36
NG_008376.3:g.3925C>T
NG_008376.4:g.4744C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-276C>T XP_011528268.1:n.-276C>T
XM_011529967.1:c.-276C>T XP_011528269.1:n.-276C>T
XM_011529968.1:c.-276C>T XP_011528270.1:n.-276C>T
XM_011529969.1:c.37+230C>T XP_011528271.1:n.37+230C>T
XM_011529970.1:c.-276C>T XP_011528272.1:n.-276C>T
XM_011529971.1:c.37+230C>T XP_011528273.1:n.37+230C>T
XM_011529972.1:c.-276C>T XP_011528274.1:n.-276C>T
XR_430455.2:n.328+379G>A
XR_002958749.1:n.275+379G>A
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