Canonical Allele Identifier: CA355379300
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1230168863

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060150G>A , CM000665.2:g.184060150G>A GRCh38
NC_000003.11:g.183777938G>A , CM000665.1:g.183777938G>A GRCh37
NC_000003.10:g.185260632G>A NCBI36
NG_012749.1:g.12104G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1142G>A MANE Select ENSP00000322617.1:p.Gly381Asp
ENST00000318351.1:c.1142G>A ENSP00000322617.1:p.Gly381Asp
NM_130770.2:c.1142G>A NP_570126.2:p.Gly381Asp
NM_130770.3:c.1142G>A MANE Select NP_570126.2:p.Gly381Asp