Canonical Allele Identifier: CA1425846976
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060124T= , CM000665.2:g.184060124T= GRCh38
NC_000003.11:g.183777912T= , CM000665.1:g.183777912T= GRCh37
NC_000003.10:g.185260606T= NCBI36
NG_012749.1:g.12078T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1142-26T= MANE Select ENSP00000322617.1:n.1142-26T=
ENST00000318351.1:c.1142-26T= ENSP00000322617.1:n.1142-26T=
NM_130770.2:c.1142-26T= NP_570126.2:n.1142-26T=
NM_130770.3:c.1142-26T= MANE Select NP_570126.2:n.1142-26T=