Canonical Allele Identifier: CA2616029220
Gene: DRD2 HGNC NCBI

Linked Data

gnomAD v4: 11-113410508-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410508C>A , CM000673.2:g.113410508C>A GRCh38
NC_000011.9:g.113281230C>A , CM000673.1:g.113281230C>A GRCh37
NC_000011.8:g.112786440C>A NCBI36
NG_008841.1:g.69772G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*219G>T MANE Select ENSP00000354859.3:n.*219G>T
ENST00000346454.7:c.*219G>T ENSP00000278597.5:n.*219G>T
ENST00000362072.7:c.*219G>T ENSP00000354859.3:n.*219G>T
ENST00000542968.5:c.*219G>T ENSP00000442172.1:n.*219G>T
ENST00000544518.5:c.*219G>T ENSP00000441068.1:n.*219G>T
NM_000795.3:c.*219G>T NP_000786.1:n.*219G>T
NM_016574.3:c.*219G>T NP_057658.2:n.*219G>T
XM_017017296.2:c.*219G>T XP_016872785.1:n.*219G>T
NM_000795.4:c.*219G>T MANE Select NP_000786.1:n.*219G>T
NM_016574.4:c.*219G>T NP_057658.2:n.*219G>T
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Search 100 bp 3'