Canonical Allele Identifier: CA679146371
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs753316384
gnomAD v3: 11-637613-G-C
gnomAD v4: 11-637613-G-C
MyVariant Identifiers: chr11:g.637613G>C (hg19) chr11:g.637613G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637613G>C , CM000673.2:g.637613G>C GRCh38
NC_000011.9:g.637613G>C , CM000673.1:g.637613G>C GRCh37
NC_000011.8:g.627613G>C NCBI36
NG_021241.1:g.5309G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.285+24G>C MANE Select ENSP00000176183.5:n.285+24G>C
ENST00000176183.5:c.285+24G>C ENSP00000176183.5:n.285+24G>C
NM_000797.3:c.285+24G>C NP_000788.2:n.285+24G>C
NM_000797.4:c.285+24G>C MANE Select NP_000788.2:n.285+24G>C
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