Canonical Allele Identifier: CA1425845485
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184056984T= , CM000665.2:g.184056984T= GRCh38
NC_000003.11:g.183774772T= , CM000665.1:g.183774772T= GRCh37
NC_000003.10:g.185257466T= NCBI36
NG_012749.1:g.8938T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.499T= MANE Select ENSP00000322617.1:p.Phe167=
ENST00000318351.1:c.499T= ENSP00000322617.1:p.Phe167=
NM_130770.2:c.499T= NP_570126.2:p.Phe167=
NM_130770.3:c.499T= MANE Select NP_570126.2:p.Phe167=