Canonical Allele Identifier: CA2725698
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs748414707

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059867G>C , CM000665.2:g.184059867G>C GRCh38
NC_000003.11:g.183777655G>C , CM000665.1:g.183777655G>C GRCh37
NC_000003.10:g.185260349G>C NCBI36
NG_012749.1:g.11821G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.965G>C MANE Select ENSP00000322617.1:p.Ser322Thr
ENST00000318351.1:c.965G>C ENSP00000322617.1:p.Ser322Thr
NM_130770.2:c.965G>C NP_570126.2:p.Ser322Thr
NM_130770.3:c.965G>C MANE Select NP_570126.2:p.Ser322Thr