Canonical Allele Identifier: CA753326795
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1419632105
MyVariant Identifiers: chr22:g.42126534C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126534C>T , CM000684.2:g.42126534C>T GRCh38
NC_000022.10:g.42522536C>T , CM000684.1:g.42522536C>T GRCh37
NC_000022.9:g.40852480C>T NCBI36
NG_008376.3:g.8458G>A
NG_008376.4:g.9277G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1332G>A ENSP00000353241.6:n.1332G>A
ENST00000645361.2:c.*40G>A MANE Select ENSP00000496150.1:n.*40G>A
ENST00000360124.9:c.1152G>A ENSP00000353241.5:n.1152G>A
ENST00000360608.9:c.*40G>A ENSP00000353820.5:n.*40G>A
ENST00000389970.7:c.*40G>A ENSP00000374620.4:n.*40G>A
NM_000106.5:c.*40G>A NP_000097.3:n.*40G>A
NM_001025161.2:c.*40G>A NP_001020332.2:n.*40G>A
XM_011529966.1:c.1452+82G>A XP_011528268.1:n.1452+82G>A
XM_011529967.1:c.1452+82G>A XP_011528269.1:n.1452+82G>A
XM_011529968.1:c.1452+82G>A XP_011528270.1:n.1452+82G>A
XM_011529969.1:c.1308+82G>A XP_011528271.1:n.1308+82G>A
XM_011529970.1:c.1299+82G>A XP_011528272.1:n.1299+82G>A
XM_011529971.1:c.*40G>A XP_011528273.1:n.*40G>A
NM_000106.6:c.*40G>A MANE Select NP_000097.3:n.*40G>A
NM_001025161.3:c.*40G>A NP_001020332.2:n.*40G>A