Canonical Allele Identifier: CA2725731
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs769662531

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060004G>A , CM000665.2:g.184060004G>A GRCh38
NC_000003.11:g.183777792G>A , CM000665.1:g.183777792G>A GRCh37
NC_000003.10:g.185260486G>A NCBI36
NG_012749.1:g.11958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1102G>A MANE Select ENSP00000322617.1:p.Gly368Arg
ENST00000318351.1:c.1102G>A ENSP00000322617.1:p.Gly368Arg
NM_130770.2:c.1102G>A NP_570126.2:p.Gly368Arg
NM_130770.3:c.1102G>A MANE Select NP_570126.2:p.Gly368Arg