Canonical Allele Identifier: CA1025920493
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1930906299

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126433A>G , CM000684.2:g.42126433A>G GRCh38
NC_000022.10:g.42522435A>G , CM000684.1:g.42522435A>G GRCh37
NC_000022.9:g.40852379A>G NCBI36
NG_008376.3:g.8559T>C
NG_008376.4:g.9378T>C

Transcript Alleles

HGVS Amino-acid change
XM_011529966.1:c.1452+183T>C XP_011528268.1:n.1452+183T>C
XM_011529967.1:c.1452+183T>C XP_011528269.1:n.1452+183T>C
XM_011529968.1:c.1452+183T>C XP_011528270.1:n.1452+183T>C
XM_011529969.1:c.1308+183T>C XP_011528271.1:n.1308+183T>C
XM_011529970.1:c.1299+183T>C XP_011528272.1:n.1299+183T>C