Canonical Allele Identifier: CA1425846980
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060135C= , CM000665.2:g.184060135C= GRCh38
NC_000003.11:g.183777923C= , CM000665.1:g.183777923C= GRCh37
NC_000003.10:g.185260617C= NCBI36
NG_012749.1:g.12089C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1142-15C= MANE Select ENSP00000322617.1:n.1142-15C=
ENST00000318351.1:c.1142-15C= ENSP00000322617.1:n.1142-15C=
NM_130770.2:c.1142-15C= NP_570126.2:n.1142-15C=
NM_130770.3:c.1142-15C= MANE Select NP_570126.2:n.1142-15C=