Canonical Allele Identifier: CA639827885

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1463095582
• gnomAD v2: 22-42522757-G-C
• gnomAD v4: 22-42126755-G-C
• MyVariant Identifiers: chr22:g.42522757G>C (hg19) ; chr22:g.42126755G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126755G>C , CM000684.2:g.42126755G>C	GRCh38
NC_000022.10:g.42522757G>C , CM000684.1:g.42522757G>C	GRCh37
NC_000022.9:g.40852701G>C	NCBI36
NG_008376.3:g.8237C>G
NG_008376.4:g.9056C>G

Transcript Alleles

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