Canonical Allele Identifier: CA355378835
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777751G>C (hg19) chr3:g.184059963G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059963G>C , CM000665.2:g.184059963G>C GRCh38
NC_000003.11:g.183777751G>C , CM000665.1:g.183777751G>C GRCh37
NC_000003.10:g.185260445G>C NCBI36
NG_012749.1:g.11917G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1061G>C MANE Select ENSP00000322617.1:p.Cys354Ser
ENST00000318351.1:c.1061G>C ENSP00000322617.1:p.Cys354Ser
NM_130770.2:c.1061G>C NP_570126.2:p.Cys354Ser
NM_130770.3:c.1061G>C MANE Select NP_570126.2:p.Cys354Ser
Search 100 bp 5'
Search 100 bp 3'