Canonical Allele Identifier: CA2657031635

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42130873-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130873T>C , CM000684.2:g.42130873T>C	GRCh38
NC_000022.10:g.42526875T>C , CM000684.1:g.42526875T>C	GRCh37
NC_000022.9:g.40856819T>C	NCBI36
NG_008376.3:g.4119A>G
NG_008376.4:g.4938A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360608.9:c.-82A>G	ENSP00000353820.5:n.-82A>G
ENST00000389970.7:c.-148A>G	ENSP00000374620.4:n.-148A>G
NM_000106.5:c.-82A>G	NP_000097.3:n.-82A>G
NM_001025161.2:c.-82A>G	NP_001020332.2:n.-82A>G
XM_011529966.1:c.-82A>G	XP_011528268.1:n.-82A>G
XM_011529967.1:c.-82A>G	XP_011528269.1:n.-82A>G
XM_011529968.1:c.-82A>G	XP_011528270.1:n.-82A>G
XM_011529969.1:c.37+424A>G	XP_011528271.1:n.37+424A>G
XM_011529970.1:c.-82A>G	XP_011528272.1:n.-82A>G
XM_011529971.1:c.37+424A>G	XP_011528273.1:n.37+424A>G
XM_011529972.1:c.-82A>G	XP_011528274.1:n.-82A>G
XR_430455.2:n.328+185T>C
XR_002958749.1:n.275+185T>C