Canonical Allele Identifier: CA437322942
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777755C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059967C>G , CM000665.2:g.184059967C>G GRCh38
NC_000003.11:g.183777755C>G , CM000665.1:g.183777755C>G GRCh37
NC_000003.10:g.185260449C>G NCBI36
NG_012749.1:g.11921C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1065C>G MANE Select ENSP00000322617.1:p.Thr355=
ENST00000318351.1:c.1065C>G ENSP00000322617.1:p.Thr355=
NM_130770.2:c.1065C>G NP_570126.2:p.Thr355=
NM_130770.3:c.1065C>G MANE Select NP_570126.2:p.Thr355=