Canonical Allele Identifier: CA472437163
Gene: DRD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.640266C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640266C>G , CM000673.2:g.640266C>G GRCh38
NC_000011.9:g.640266C>G , CM000673.1:g.640266C>G GRCh37
NC_000011.8:g.630266C>G NCBI36
NG_021241.1:g.7962C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1017C>G MANE Select ENSP00000176183.5:p.Gly339=
ENST00000176183.5:c.1017C>G ENSP00000176183.5:p.Gly339=
NM_000797.3:c.1017C>G NP_000788.2:p.Gly339=
NM_000797.4:c.1017C>G MANE Select NP_000788.2:p.Gly339=