Canonical Allele Identifier: CA382649104

Gene: DRD2

Linked Data

• gnomAD v3: 11-113410810-C-A
• gnomAD v4: 11-113410810-C-A
• MyVariant Identifiers: chr11:g.113281532C>A (hg19) ; chr11:g.113410810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410810C>A , CM000673.2:g.113410810C>A	GRCh38
NC_000011.9:g.113281532C>A , CM000673.1:g.113281532C>A	GRCh37
NC_000011.8:g.112786742C>A	NCBI36
NG_008841.1:g.69470G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1249G>T MANE Select	ENSP00000354859.3:p.Val417Phe
ENST00000346454.7:c.1162G>T	ENSP00000278597.5:p.Val388Phe
ENST00000362072.7:c.1249G>T	ENSP00000354859.3:p.Val417Phe
ENST00000538967.5:c.1255G>T	ENSP00000438215.1:p.Val419Phe
ENST00000542968.5:c.1249G>T	ENSP00000442172.1:p.Val417Phe
ENST00000544518.5:c.1246G>T	ENSP00000441068.1:p.Val416Phe
NM_000795.3:c.1249G>T	NP_000786.1:p.Val417Phe
NM_016574.3:c.1162G>T	NP_057658.2:p.Val388Phe
XM_017017296.2:c.1249G>T	XP_016872785.1:p.Val417Phe
NM_000795.4:c.1249G>T MANE Select	NP_000786.1:p.Val417Phe
NM_016574.4:c.1162G>T	NP_057658.2:p.Val388Phe