Canonical Allele Identifier: CA753326715
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1342428583
MyVariant Identifiers: chr22:g.42126415G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126415G>A , CM000684.2:g.42126415G>A GRCh38
NC_000022.10:g.42522417G>A , CM000684.1:g.42522417G>A GRCh37
NC_000022.9:g.40852361G>A NCBI36
NG_008376.3:g.8577C>T
NG_008376.4:g.9396C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1452+201C>T XP_011528268.1:n.1452+201C>T
XM_011529967.1:c.1452+201C>T XP_011528269.1:n.1452+201C>T
XM_011529968.1:c.1452+201C>T XP_011528270.1:n.1452+201C>T
XM_011529969.1:c.1308+201C>T XP_011528271.1:n.1308+201C>T
XM_011529970.1:c.1299+201C>T XP_011528272.1:n.1299+201C>T