Canonical Allele Identifier: CA355380111
Gene: HTR3C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060318C>T , CM000665.2:g.184060318C>T GRCh38
NC_000003.11:g.183778106C>T , CM000665.1:g.183778106C>T GRCh37
NC_000003.10:g.185260800C>T NCBI36
NG_012749.1:g.12272C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1310C>T MANE Select ENSP00000322617.1:p.Ser437Phe
ENST00000318351.1:c.1310C>T ENSP00000322617.1:p.Ser437Phe
NM_130770.2:c.1310C>T NP_570126.2:p.Ser437Phe
NM_130770.3:c.1310C>T MANE Select NP_570126.2:p.Ser437Phe