Canonical Allele Identifier: CA1425845480
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184056978G= , CM000665.2:g.184056978G= GRCh38
NC_000003.11:g.183774766G= , CM000665.1:g.183774766G= GRCh37
NC_000003.10:g.185257460G= NCBI36
NG_012749.1:g.8932G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.493G= MANE Select ENSP00000322617.1:p.Asp165=
ENST00000318351.1:c.493G= ENSP00000322617.1:p.Asp165=
NM_130770.2:c.493G= NP_570126.2:p.Asp165=
NM_130770.3:c.493G= MANE Select NP_570126.2:p.Asp165=