Canonical Allele Identifier: CA753332174
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1398343256
MyVariant Identifiers: chr22:g.42131072T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42131072T>C , CM000684.2:g.42131072T>C GRCh38
NC_000022.10:g.42527074T>C , CM000684.1:g.42527074T>C GRCh37
NC_000022.9:g.40857018T>C NCBI36
NG_008376.3:g.3920A>G
NG_008376.4:g.4739A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.-281A>G XP_011528268.1:n.-281A>G
XM_011529967.1:c.-281A>G XP_011528269.1:n.-281A>G
XM_011529968.1:c.-281A>G XP_011528270.1:n.-281A>G
XM_011529969.1:c.37+225A>G XP_011528271.1:n.37+225A>G
XM_011529970.1:c.-281A>G XP_011528272.1:n.-281A>G
XM_011529971.1:c.37+225A>G XP_011528273.1:n.37+225A>G
XM_011529972.1:c.-281A>G XP_011528274.1:n.-281A>G
XR_430455.2:n.328+384T>C
XR_002958749.1:n.275+384T>C