Canonical Allele Identifier: CA379002789

Gene: DRD4

Linked Data

• dbSNP Id: rs1377082826
• gnomAD v3: 11-637549-T-C
• gnomAD v4: 11-637549-T-C
• MyVariant Identifiers: chr11:g.637549T>C (hg19) ; chr11:g.637549T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.637549T>C , CM000673.2:g.637549T>C	GRCh38
NC_000011.9:g.637549T>C , CM000673.1:g.637549T>C	GRCh37
NC_000011.8:g.627549T>C	NCBI36
NG_021241.1:g.5245T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176183.6:c.245T>C MANE Select	ENSP00000176183.5:p.Leu82Pro
ENST00000176183.5:c.245T>C	ENSP00000176183.5:p.Leu82Pro
NM_000797.3:c.245T>C	NP_000788.2:p.Leu82Pro
NM_000797.4:c.245T>C MANE Select	NP_000788.2:p.Leu82Pro