Canonical Allele Identifier: CA2406577717
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1930911127
gnomAD v4: 22-42126468-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126468T>G , CM000684.2:g.42126468T>G GRCh38
NC_000022.10:g.42522470T>G , CM000684.1:g.42522470T>G GRCh37
NC_000022.9:g.40852414T>G NCBI36
NG_008376.3:g.8524A>C
NG_008376.4:g.9343A>C

Transcript Alleles

HGVS Amino-acid change
XM_011529966.1:c.1452+148A>C XP_011528268.1:n.1452+148A>C
XM_011529967.1:c.1452+148A>C XP_011528269.1:n.1452+148A>C
XM_011529968.1:c.1452+148A>C XP_011528270.1:n.1452+148A>C
XM_011529969.1:c.1308+148A>C XP_011528271.1:n.1308+148A>C
XM_011529970.1:c.1299+148A>C XP_011528272.1:n.1299+148A>C
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