Canonical Allele Identifier: CA88838143
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs6766410

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184056974C>T , CM000665.2:g.184056974C>T GRCh38
NC_000003.11:g.183774762C>T , CM000665.1:g.183774762C>T GRCh37
NC_000003.10:g.185257456C>T NCBI36
NG_012749.1:g.8928C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.489C>T MANE Select ENSP00000322617.1:p.Asn163=
ENST00000318351.1:c.489C>T ENSP00000322617.1:p.Asn163=
NM_130770.2:c.489C>T NP_570126.2:p.Asn163=
NM_130770.3:c.489C>T MANE Select NP_570126.2:p.Asn163=