Canonical Allele Identifier: CA1425846996
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060167G= , CM000665.2:g.184060167G= GRCh38
NC_000003.11:g.183777955G= , CM000665.1:g.183777955G= GRCh37
NC_000003.10:g.185260649G= NCBI36
NG_012749.1:g.12121G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1159G= MANE Select ENSP00000322617.1:p.Glu387=
ENST00000318351.1:c.1159G= ENSP00000322617.1:p.Glu387=
NM_130770.2:c.1159G= NP_570126.2:p.Glu387=
NM_130770.3:c.1159G= MANE Select NP_570126.2:p.Glu387=