Canonical Allele Identifier: CA411772780

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42127940-C-G
• MyVariant Identifiers: chr22:g.42523942C>G (hg19) ; chr22:g.42127940C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127940C>G , CM000684.2:g.42127940C>G	GRCh38
NC_000022.10:g.42523942C>G , CM000684.1:g.42523942C>G	GRCh37
NC_000022.9:g.40853886C>G	NCBI36
NG_008376.3:g.7052G>C
NG_008376.4:g.7871G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.691-6G>C	ENSP00000353241.6:n.691-6G>C
ENST00000645361.2:c.887G>C MANE Select	ENSP00000496150.1:p.Arg296Pro
ENST00000359033.4:c.734G>C	ENSP00000351927.4:p.Arg245Pro
ENST00000360124.9:c.511-6G>C	ENSP00000353241.5:n.511-6G>C
ENST00000360608.9:c.887G>C	ENSP00000353820.5:p.Arg296Pro
ENST00000389970.7:c.821G>C	ENSP00000374620.4:p.Arg274Pro
ENST00000488442.1:n.1611G>C
NM_000106.5:c.887G>C	NP_000097.3:p.Arg296Pro
NM_001025161.2:c.734G>C	NP_001020332.2:p.Arg245Pro
XM_011529966.1:c.887G>C	XP_011528268.1:p.Arg296Pro
XM_011529967.1:c.887G>C	XP_011528269.1:p.Arg296Pro
XM_011529968.1:c.887G>C	XP_011528270.1:p.Arg296Pro
XM_011529969.1:c.743G>C	XP_011528271.1:p.Arg248Pro
XM_011529970.1:c.734G>C	XP_011528272.1:p.Arg245Pro
XM_011529971.1:c.743G>C	XP_011528273.1:p.Arg248Pro
XM_011529972.1:c.843+234G>C	XP_011528274.1:n.843+234G>C
NM_000106.6:c.887G>C MANE Select	NP_000097.3:p.Arg296Pro
NM_001025161.3:c.734G>C	NP_001020332.2:p.Arg245Pro