Canonical Allele Identifier: CA355379407

Gene: HTR3C

Linked Data

• COSMIC: COSM5398739
• MyVariant Identifiers: chr3:g.183777965G>A (hg19) ; chr3:g.184060177G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060177G>A , CM000665.2:g.184060177G>A	GRCh38
NC_000003.11:g.183777965G>A , CM000665.1:g.183777965G>A	GRCh37
NC_000003.10:g.185260659G>A	NCBI36
NG_012749.1:g.12131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1169G>A MANE Select	ENSP00000322617.1:p.Gly390Glu
ENST00000318351.1:c.1169G>A	ENSP00000322617.1:p.Gly390Glu
NM_130770.2:c.1169G>A	NP_570126.2:p.Gly390Glu
NM_130770.3:c.1169G>A MANE Select	NP_570126.2:p.Gly390Glu