Canonical Allele Identifier: CA411772859

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523975T>G (hg19) ; chr22:g.42127973T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127973T>G , CM000684.2:g.42127973T>G	GRCh38
NC_000022.10:g.42523975T>G , CM000684.1:g.42523975T>G	GRCh37
NC_000022.9:g.40853919T>G	NCBI36
NG_008376.3:g.7019A>C
NG_008376.4:g.7838A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.691-39A>C	ENSP00000353241.6:n.691-39A>C
ENST00000645361.2:c.854A>C MANE Select	ENSP00000496150.1:p.Asn285Thr
ENST00000359033.4:c.701A>C	ENSP00000351927.4:p.Asn234Thr
ENST00000360124.9:c.511-39A>C	ENSP00000353241.5:n.511-39A>C
ENST00000360608.9:c.854A>C	ENSP00000353820.5:p.Asn285Thr
ENST00000389970.7:c.788A>C	ENSP00000374620.4:p.Asn263Thr
ENST00000488442.1:n.1578A>C
NM_000106.5:c.854A>C	NP_000097.3:p.Asn285Thr
NM_001025161.2:c.701A>C	NP_001020332.2:p.Asn234Thr
XM_011529966.1:c.854A>C	XP_011528268.1:p.Asn285Thr
XM_011529967.1:c.854A>C	XP_011528269.1:p.Asn285Thr
XM_011529968.1:c.854A>C	XP_011528270.1:p.Asn285Thr
XM_011529969.1:c.710A>C	XP_011528271.1:p.Asn237Thr
XM_011529970.1:c.701A>C	XP_011528272.1:p.Asn234Thr
XM_011529971.1:c.710A>C	XP_011528273.1:p.Asn237Thr
XM_011529972.1:c.843+201A>C	XP_011528274.1:n.843+201A>C
NM_000106.6:c.854A>C MANE Select	NP_000097.3:p.Asn285Thr
NM_001025161.3:c.701A>C	NP_001020332.2:p.Asn234Thr