Canonical Allele Identifier: CA355378988
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs143287242

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1091C>G MANE Select ENSP00000322617.1:p.Ala364Gly
ENST00000318351.1:c.1091C>G ENSP00000322617.1:p.Ala364Gly
NM_130770.2:c.1091C>G NP_570126.2:p.Ala364Gly
NM_130770.3:c.1091C>G MANE Select NP_570126.2:p.Ala364Gly