Canonical Allele Identifier: CA2704746091

Gene: HTR3C

Linked Data

• dbSNP Id: rs1269894799

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060104C>G , CM000665.2:g.184060104C>G	GRCh38
NC_000003.11:g.183777892C>G , CM000665.1:g.183777892C>G	GRCh37
NC_000003.10:g.185260586C>G	NCBI36
NG_012749.1:g.12058C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142-46C>G MANE Select	ENSP00000322617.1:n.1142-46C>G
ENST00000318351.1:c.1142-46C>G	ENSP00000322617.1:n.1142-46C>G
NM_130770.2:c.1142-46C>G	NP_570126.2:n.1142-46C>G
NM_130770.3:c.1142-46C>G MANE Select	NP_570126.2:n.1142-46C>G