Canonical Allele Identifier: CA411769816
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42522612G>T (hg19) chr22:g.42126610G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126610G>T , CM000684.2:g.42126610G>T GRCh38
NC_000022.10:g.42522612G>T , CM000684.1:g.42522612G>T GRCh37
NC_000022.9:g.40852556G>T NCBI36
NG_008376.3:g.8382C>A
NG_008376.4:g.9201C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1256C>A ENSP00000353241.6:n.1256C>A
ENST00000645361.2:c.1458C>A MANE Select ENSP00000496150.1:p.Ser486Arg
ENST00000359033.4:c.1305C>A ENSP00000351927.4:p.Ser435Arg
ENST00000360124.9:c.1076C>A ENSP00000353241.5:n.1076C>A
ENST00000360608.9:c.1458C>A ENSP00000353820.5:p.Ser486Arg
ENST00000389970.7:c.1449C>A ENSP00000374620.4:p.Ser483Arg
ENST00000488442.1:n.2182C>A
NM_000106.5:c.1458C>A NP_000097.3:p.Ser486Arg
NM_001025161.2:c.1305C>A NP_001020332.2:p.Ser435Arg
XM_011529966.1:c.1452+6C>A XP_011528268.1:n.1452+6C>A
XM_011529967.1:c.1452+6C>A XP_011528269.1:n.1452+6C>A
XM_011529968.1:c.1452+6C>A XP_011528270.1:n.1452+6C>A
XM_011529969.1:c.1308+6C>A XP_011528271.1:n.1308+6C>A
XM_011529970.1:c.1299+6C>A XP_011528272.1:n.1299+6C>A
XM_011529971.1:c.1314C>A XP_011528273.1:p.Ser438Arg
NM_000106.6:c.1458C>A MANE Select NP_000097.3:p.Ser486Arg
NM_001025161.3:c.1305C>A NP_001020332.2:p.Ser435Arg
Search 100 bp 5'
Search 100 bp 3'