Canonical Allele Identifier: CA411770092

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522754C>G (hg19) ; chr22:g.42126752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126752C>G , CM000684.2:g.42126752C>G	GRCh38
NC_000022.10:g.42522754C>G , CM000684.1:g.42522754C>G	GRCh37
NC_000022.9:g.40852698C>G	NCBI36
NG_008376.3:g.8240G>C
NG_008376.4:g.9059G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1114G>C	ENSP00000353241.6:n.1114G>C
ENST00000645361.2:c.1316G>C MANE Select	ENSP00000496150.1:p.Gly439Ala
ENST00000359033.4:c.1163G>C	ENSP00000351927.4:p.Gly388Ala
ENST00000360124.9:c.934G>C	ENSP00000353241.5:n.934G>C
ENST00000360608.9:c.1316G>C	ENSP00000353820.5:p.Gly439Ala
ENST00000389970.7:c.1307G>C	ENSP00000374620.4:p.Gly436Ala
ENST00000488442.1:n.2040G>C
NM_000106.5:c.1316G>C	NP_000097.3:p.Gly439Ala
NM_001025161.2:c.1163G>C	NP_001020332.2:p.Gly388Ala
XM_011529966.1:c.1316G>C	XP_011528268.1:p.Gly439Ala
XM_011529967.1:c.1316G>C	XP_011528269.1:p.Gly439Ala
XM_011529968.1:c.1316G>C	XP_011528270.1:p.Gly439Ala
XM_011529969.1:c.1172G>C	XP_011528271.1:p.Gly391Ala
XM_011529970.1:c.1163G>C	XP_011528272.1:p.Gly388Ala
XM_011529971.1:c.1172G>C	XP_011528273.1:p.Gly391Ala
NM_000106.6:c.1316G>C MANE Select	NP_000097.3:p.Gly439Ala
NM_001025161.3:c.1163G>C	NP_001020332.2:p.Gly388Ala