Canonical Allele Identifier: CA411772624

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931203893
• MyVariant Identifiers: chr22:g.42523916C>G (hg19) ; chr22:g.42127914C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127914C>G , CM000684.2:g.42127914C>G	GRCh38
NC_000022.10:g.42523916C>G , CM000684.1:g.42523916C>G	GRCh37
NC_000022.9:g.40853860C>G	NCBI36
NG_008376.3:g.7078G>C
NG_008376.4:g.7897G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.711G>C	ENSP00000353241.6:p.Leu237=
ENST00000645361.2:c.913G>C MANE Select	ENSP00000496150.1:p.Ala305Pro
ENST00000359033.4:c.760G>C	ENSP00000351927.4:p.Ala254Pro
ENST00000360124.9:c.531G>C	ENSP00000353241.5:p.Leu177=
ENST00000360608.9:c.913G>C	ENSP00000353820.5:p.Ala305Pro
ENST00000389970.7:c.847G>C	ENSP00000374620.4:p.Ala283Pro
ENST00000488442.1:n.1637G>C
NM_000106.5:c.913G>C	NP_000097.3:p.Ala305Pro
NM_001025161.2:c.760G>C	NP_001020332.2:p.Ala254Pro
XM_011529966.1:c.913G>C	XP_011528268.1:p.Ala305Pro
XM_011529967.1:c.913G>C	XP_011528269.1:p.Ala305Pro
XM_011529968.1:c.913G>C	XP_011528270.1:p.Ala305Pro
XM_011529969.1:c.769G>C	XP_011528271.1:p.Ala257Pro
XM_011529970.1:c.760G>C	XP_011528272.1:p.Ala254Pro
XM_011529971.1:c.769G>C	XP_011528273.1:p.Ala257Pro
XM_011529972.1:c.843+260G>C	XP_011528274.1:n.843+260G>C
NM_000106.6:c.913G>C MANE Select	NP_000097.3:p.Ala305Pro
NM_001025161.3:c.760G>C	NP_001020332.2:p.Ala254Pro