Canonical Allele Identifier: CA411775947

Gene: CYP2D6

Linked Data

• dbSNP Id: rs28371696
• MyVariant Identifiers: chr22:g.42526717C>G (hg19) ; chr22:g.42130715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130715C>G , CM000684.2:g.42130715C>G	GRCh38
NC_000022.10:g.42526717C>G , CM000684.1:g.42526717C>G	GRCh37
NC_000022.9:g.40856661C>G	NCBI36
NG_008376.3:g.4277G>C
NG_008376.4:g.5096G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.77G>C	ENSP00000353241.6:p.Arg26Pro
ENST00000645361.2:c.77G>C MANE Select	ENSP00000496150.1:p.Arg26Pro
ENST00000359033.4:c.77G>C	ENSP00000351927.4:p.Arg26Pro
ENST00000360608.9:c.77G>C	ENSP00000353820.5:p.Arg26Pro
ENST00000389970.7:c.11G>C	ENSP00000374620.4:p.Arg4Pro
ENST00000488442.1:n.99G>C
NM_000106.5:c.77G>C	NP_000097.3:p.Arg26Pro
NM_001025161.2:c.77G>C	NP_001020332.2:p.Arg26Pro
XM_011529966.1:c.77G>C	XP_011528268.1:p.Arg26Pro
XM_011529967.1:c.77G>C	XP_011528269.1:p.Arg26Pro
XM_011529968.1:c.77G>C	XP_011528270.1:p.Arg26Pro
XM_011529969.1:c.37+582G>C	XP_011528271.1:n.37+582G>C
XM_011529970.1:c.77G>C	XP_011528272.1:p.Arg26Pro
XM_011529971.1:c.37+582G>C	XP_011528273.1:n.37+582G>C
XM_011529972.1:c.77G>C	XP_011528274.1:p.Arg26Pro
XR_430455.2:n.328+27C>G
NM_000106.6:c.77G>C MANE Select	NP_000097.3:p.Arg26Pro
XR_002958749.1:n.275+27C>G
NM_001025161.3:c.77G>C	NP_001020332.2:p.Arg26Pro