Canonical Allele Identifier: CA411774131

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146937515
• MyVariant Identifiers: chr22:g.42524937A>G (hg19) ; chr22:g.42128935A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128935A>G , CM000684.2:g.42128935A>G	GRCh38
NC_000022.10:g.42524937A>G , CM000684.1:g.42524937A>G	GRCh37
NC_000022.9:g.40854881A>G	NCBI36
NG_008376.3:g.6057T>C
NG_008376.4:g.6876T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.362T>C	ENSP00000353241.6:p.Phe121Ser
ENST00000645361.2:c.515T>C MANE Select	ENSP00000496150.1:p.Phe172Ser
ENST00000359033.4:c.362T>C	ENSP00000351927.4:p.Phe121Ser
ENST00000360124.9:c.182T>C	ENSP00000353241.5:p.Phe61Ser
ENST00000360608.9:c.515T>C	ENSP00000353820.5:p.Phe172Ser
ENST00000389970.7:c.449T>C	ENSP00000374620.4:p.Phe150Ser
ENST00000488442.1:n.1239T>C
NM_000106.5:c.515T>C	NP_000097.3:p.Phe172Ser
NM_001025161.2:c.362T>C	NP_001020332.2:p.Phe121Ser
XM_011529966.1:c.515T>C	XP_011528268.1:p.Phe172Ser
XM_011529967.1:c.515T>C	XP_011528269.1:p.Phe172Ser
XM_011529968.1:c.515T>C	XP_011528270.1:p.Phe172Ser
XM_011529969.1:c.371T>C	XP_011528271.1:p.Phe124Ser
XM_011529970.1:c.362T>C	XP_011528272.1:p.Phe121Ser
XM_011529971.1:c.371T>C	XP_011528273.1:p.Phe124Ser
XM_011529972.1:c.515T>C	XP_011528274.1:p.Phe172Ser
NM_000106.6:c.515T>C MANE Select	NP_000097.3:p.Phe172Ser
NM_001025161.3:c.362T>C	NP_001020332.2:p.Phe121Ser