Canonical Allele Identifier: CA382650258
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412756T>A , CM000673.2:g.113412756T>A GRCh38
NC_000011.9:g.113283478T>A , CM000673.1:g.113283478T>A GRCh37
NC_000011.8:g.112788688T>A NCBI36
NG_008841.1:g.67524A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.938A>T MANE Select ENSP00000354859.3:p.His313Leu
ENST00000346454.7:c.851A>T ENSP00000278597.5:p.His284Leu
ENST00000362072.7:c.938A>T ENSP00000354859.3:p.His313Leu
ENST00000538967.5:c.944A>T ENSP00000438215.1:p.His315Leu
ENST00000542968.5:c.938A>T ENSP00000442172.1:p.His313Leu
ENST00000544518.5:c.935A>T ENSP00000441068.1:p.His312Leu
NM_000795.3:c.938A>T NP_000786.1:p.His313Leu
NM_016574.3:c.851A>T NP_057658.2:p.His284Leu
XM_017017296.2:c.938A>T XP_016872785.1:p.His313Leu
NM_000795.4:c.938A>T MANE Select NP_000786.1:p.His313Leu
NM_016574.4:c.851A>T NP_057658.2:p.His284Leu