Canonical Allele Identifier: CA382649090

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281526T>G (hg19) ; chr11:g.113410804T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410804T>G , CM000673.2:g.113410804T>G	GRCh38
NC_000011.9:g.113281526T>G , CM000673.1:g.113281526T>G	GRCh37
NC_000011.8:g.112786736T>G	NCBI36
NG_008841.1:g.69476A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1255A>C MANE Select	ENSP00000354859.3:p.Ser419Arg
ENST00000346454.7:c.1168A>C	ENSP00000278597.5:p.Ser390Arg
ENST00000362072.7:c.1255A>C	ENSP00000354859.3:p.Ser419Arg
ENST00000538967.5:c.1261A>C	ENSP00000438215.1:p.Ser421Arg
ENST00000542968.5:c.1255A>C	ENSP00000442172.1:p.Ser419Arg
ENST00000544518.5:c.1252A>C	ENSP00000441068.1:p.Ser418Arg
NM_000795.3:c.1255A>C	NP_000786.1:p.Ser419Arg
NM_016574.3:c.1168A>C	NP_057658.2:p.Ser390Arg
XM_017017296.2:c.1255A>C	XP_016872785.1:p.Ser419Arg
NM_000795.4:c.1255A>C MANE Select	NP_000786.1:p.Ser419Arg
NM_016574.4:c.1168A>C	NP_057658.2:p.Ser390Arg