Canonical Allele Identifier: CA355380047

Gene: HTR3C

Linked Data

• MyVariant Identifiers: chr3:g.183778091T>G (hg19) ; chr3:g.184060303T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060303T>G , CM000665.2:g.184060303T>G	GRCh38
NC_000003.11:g.183778091T>G , CM000665.1:g.183778091T>G	GRCh37
NC_000003.10:g.185260785T>G	NCBI36
NG_012749.1:g.12257T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1295T>G MANE Select	ENSP00000322617.1:p.Leu432Arg
ENST00000318351.1:c.1295T>G	ENSP00000322617.1:p.Leu432Arg
NM_130770.2:c.1295T>G	NP_570126.2:p.Leu432Arg
NM_130770.3:c.1295T>G MANE Select	NP_570126.2:p.Leu432Arg