Canonical Allele Identifier: CA1425846997
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060171T= , CM000665.2:g.184060171T= GRCh38
NC_000003.11:g.183777959T= , CM000665.1:g.183777959T= GRCh37
NC_000003.10:g.185260653T= NCBI36
NG_012749.1:g.12125T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1163T= MANE Select ENSP00000322617.1:p.Leu388=
ENST00000318351.1:c.1163T= ENSP00000322617.1:p.Leu388=
NM_130770.2:c.1163T= NP_570126.2:p.Leu388=
NM_130770.3:c.1163T= MANE Select NP_570126.2:p.Leu388=