Canonical Allele Identifier: CA1025920530
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1930922262

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126512A>G , CM000684.2:g.42126512A>G GRCh38
NC_000022.10:g.42522514A>G , CM000684.1:g.42522514A>G GRCh37
NC_000022.9:g.40852458A>G NCBI36
NG_008376.3:g.8480T>C
NG_008376.4:g.9299T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1354T>C ENSP00000353241.6:n.1354T>C
ENST00000645361.2:c.*62T>C MANE Select ENSP00000496150.1:n.*62T>C
ENST00000360124.9:c.1174T>C ENSP00000353241.5:n.1174T>C
ENST00000360608.9:c.*62T>C ENSP00000353820.5:n.*62T>C
ENST00000389970.7:c.*62T>C ENSP00000374620.4:n.*62T>C
NM_000106.5:c.*62T>C NP_000097.3:n.*62T>C
NM_001025161.2:c.*62T>C NP_001020332.2:n.*62T>C
XM_011529966.1:c.1452+104T>C XP_011528268.1:n.1452+104T>C
XM_011529967.1:c.1452+104T>C XP_011528269.1:n.1452+104T>C
XM_011529968.1:c.1452+104T>C XP_011528270.1:n.1452+104T>C
XM_011529969.1:c.1308+104T>C XP_011528271.1:n.1308+104T>C
XM_011529970.1:c.1299+104T>C XP_011528272.1:n.1299+104T>C
XM_011529971.1:c.*62T>C XP_011528273.1:n.*62T>C
NM_000106.6:c.*62T>C MANE Select NP_000097.3:n.*62T>C
NM_001025161.3:c.*62T>C NP_001020332.2:n.*62T>C