Canonical Allele Identifier: CA2725748

Gene: HTR3C

Linked Data

• dbSNP Id: rs769419921
• ExAC: 3:183777914 A / C
• gnomAD v2: 3-183777914-A-C
• MyVariant Identifiers: chr3:g.183777914A>C (hg19) ; chr3:g.184060126A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060126A>C , CM000665.2:g.184060126A>C	GRCh38
NC_000003.11:g.183777914A>C , CM000665.1:g.183777914A>C	GRCh37
NC_000003.10:g.185260608A>C	NCBI36
NG_012749.1:g.12080A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142-24A>C MANE Select	ENSP00000322617.1:n.1142-24A>C
ENST00000318351.1:c.1142-24A>C	ENSP00000322617.1:n.1142-24A>C
NM_130770.2:c.1142-24A>C	NP_570126.2:n.1142-24A>C
NM_130770.3:c.1142-24A>C MANE Select	NP_570126.2:n.1142-24A>C