Canonical Allele Identifier: CA437323022
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777812C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060024C>T , CM000665.2:g.184060024C>T GRCh38
NC_000003.11:g.183777812C>T , CM000665.1:g.183777812C>T GRCh37
NC_000003.10:g.185260506C>T NCBI36
NG_012749.1:g.11978C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1122C>T MANE Select ENSP00000322617.1:p.Leu374=
ENST00000318351.1:c.1122C>T ENSP00000322617.1:p.Leu374=
NM_130770.2:c.1122C>T NP_570126.2:p.Leu374=
NM_130770.3:c.1122C>T MANE Select NP_570126.2:p.Leu374=