Canonical Allele Identifier: CA355379436

Gene: HTR3C

Linked Data

• MyVariant Identifiers: chr3:g.183777979C>A (hg19) ; chr3:g.184060191C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060191C>A , CM000665.2:g.184060191C>A	GRCh38
NC_000003.11:g.183777979C>A , CM000665.1:g.183777979C>A	GRCh37
NC_000003.10:g.185260673C>A	NCBI36
NG_012749.1:g.12145C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1183C>A MANE Select	ENSP00000322617.1:p.Pro395Thr
ENST00000318351.1:c.1183C>A	ENSP00000322617.1:p.Pro395Thr
NM_130770.2:c.1183C>A	NP_570126.2:p.Pro395Thr
NM_130770.3:c.1183C>A MANE Select	NP_570126.2:p.Pro395Thr