Canonical Allele Identifier: CA2725747

Gene: HTR3C

Linked Data

• dbSNP Id: rs372139110
• ExAC: 3:183777912 T / C
• gnomAD v2: 3-183777912-T-C
• gnomAD v3: 3-184060124-T-C
• gnomAD v4: 3-184060124-T-C
• MyVariant Identifiers: chr3:g.183777912T>C (hg19) ; chr3:g.184060124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060124T>C , CM000665.2:g.184060124T>C	GRCh38
NC_000003.11:g.183777912T>C , CM000665.1:g.183777912T>C	GRCh37
NC_000003.10:g.185260606T>C	NCBI36
NG_012749.1:g.12078T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142-26T>C MANE Select	ENSP00000322617.1:n.1142-26T>C
ENST00000318351.1:c.1142-26T>C	ENSP00000322617.1:n.1142-26T>C
NM_130770.2:c.1142-26T>C	NP_570126.2:n.1142-26T>C
NM_130770.3:c.1142-26T>C MANE Select	NP_570126.2:n.1142-26T>C