Canonical Allele Identifier: CA355379296

Gene: HTR3C

Linked Data

• dbSNP Id: rs1230168863
• gnomAD v2: 3-183777938-G-T
• gnomAD v4: 3-184060150-G-T
• MyVariant Identifiers: chr3:g.183777938G>T (hg19) ; chr3:g.184060150G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060150G>T , CM000665.2:g.184060150G>T	GRCh38
NC_000003.11:g.183777938G>T , CM000665.1:g.183777938G>T	GRCh37
NC_000003.10:g.185260632G>T	NCBI36
NG_012749.1:g.12104G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142G>T MANE Select	ENSP00000322617.1:p.Gly381Val
ENST00000318351.1:c.1142G>T	ENSP00000322617.1:p.Gly381Val
NM_130770.2:c.1142G>T	NP_570126.2:p.Gly381Val
NM_130770.3:c.1142G>T MANE Select	NP_570126.2:p.Gly381Val