Canonical Allele Identifier: CA2725745
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs768203994

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060110C>T , CM000665.2:g.184060110C>T GRCh38
NC_000003.11:g.183777898C>T , CM000665.1:g.183777898C>T GRCh37
NC_000003.10:g.185260592C>T NCBI36
NG_012749.1:g.12064C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1142-40C>T MANE Select ENSP00000322617.1:n.1142-40C>T
ENST00000318351.1:c.1142-40C>T ENSP00000322617.1:n.1142-40C>T
NM_130770.2:c.1142-40C>T NP_570126.2:n.1142-40C>T
NM_130770.3:c.1142-40C>T MANE Select NP_570126.2:n.1142-40C>T