Canonical Allele Identifier: CA903679509

Gene: HTR3C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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