Canonical Allele Identifier: CA639488537
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1285632300

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126345C>T , CM000684.2:g.42126345C>T GRCh38
NC_000022.10:g.42522347C>T , CM000684.1:g.42522347C>T GRCh37
NC_000022.9:g.40852291C>T NCBI36
NG_008376.3:g.8647G>A
NG_008376.4:g.9466G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1452+271G>A XP_011528268.1:n.1452+271G>A
XM_011529967.1:c.1452+271G>A XP_011528269.1:n.1452+271G>A
XM_011529968.1:c.1452+271G>A XP_011528270.1:n.1452+271G>A
XM_011529969.1:c.1308+271G>A XP_011528271.1:n.1308+271G>A
XM_011529970.1:c.1299+271G>A XP_011528272.1:n.1299+271G>A