Canonical Allele Identifier: CA1425846907
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059993C= , CM000665.2:g.184059993C= GRCh38
NC_000003.11:g.183777781C= , CM000665.1:g.183777781C= GRCh37
NC_000003.10:g.185260475C= NCBI36
NG_012749.1:g.11947C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1091C= MANE Select ENSP00000322617.1:p.Ala364=
ENST00000318351.1:c.1091C= ENSP00000322617.1:p.Ala364=
NM_130770.2:c.1091C= NP_570126.2:p.Ala364=
NM_130770.3:c.1091C= MANE Select NP_570126.2:p.Ala364=