Canonical Allele Identifier: CA1425846998
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060172A= , CM000665.2:g.184060172A= GRCh38
NC_000003.11:g.183777960A= , CM000665.1:g.183777960A= GRCh37
NC_000003.10:g.185260654A= NCBI36
NG_012749.1:g.12126A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1164A= MANE Select ENSP00000322617.1:p.Leu388=
ENST00000318351.1:c.1164A= ENSP00000322617.1:p.Leu388=
NM_130770.2:c.1164A= NP_570126.2:p.Leu388=
NM_130770.3:c.1164A= MANE Select NP_570126.2:p.Leu388=