Canonical Allele Identifier: CA2725749

Gene: HTR3C

Linked Data

• dbSNP Id: rs6807271
• ExAC: 3:183777919 G / A
• gnomAD v2: 3-183777919-G-A
• gnomAD v3: 3-184060131-G-A
• gnomAD v4: 3-184060131-G-A
• MyVariant Identifiers: chr3:g.183777919G>A (hg19) ; chr3:g.184060131G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060131G>A , CM000665.2:g.184060131G>A	GRCh38
NC_000003.11:g.183777919G>A , CM000665.1:g.183777919G>A	GRCh37
NC_000003.10:g.185260613G>A	NCBI36
NG_012749.1:g.12085G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142-19G>A MANE Select	ENSP00000322617.1:n.1142-19G>A
ENST00000318351.1:c.1142-19G>A	ENSP00000322617.1:n.1142-19G>A
NM_130770.2:c.1142-19G>A	NP_570126.2:n.1142-19G>A
NM_130770.3:c.1142-19G>A MANE Select	NP_570126.2:n.1142-19G>A