Canonical Allele Identifier: CA2725782
Gene: HTR3C HGNC NCBI

Linked Data

ClinVar Variation Id: 3107536
ClinVar RCV Id: RCV004397369
dbSNP Id: rs755499061
ExAC: 3:183778039 T / C
gnomAD v2: 3-183778039-T-C
gnomAD v3: 3-184060251-T-C
gnomAD v4: 3-184060251-T-C
MyVariant Identifiers: chr3:g.183778039T>C (hg19) chr3:g.184060251T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060251T>C , CM000665.2:g.184060251T>C GRCh38
NC_000003.11:g.183778039T>C , CM000665.1:g.183778039T>C GRCh37
NC_000003.10:g.185260733T>C NCBI36
NG_012749.1:g.12205T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1243T>C MANE Select ENSP00000322617.1:p.Trp415Arg
ENST00000318351.1:c.1243T>C ENSP00000322617.1:p.Trp415Arg
NM_130770.2:c.1243T>C NP_570126.2:p.Trp415Arg
NM_130770.3:c.1243T>C MANE Select NP_570126.2:p.Trp415Arg
Search 100 bp 5'
Search 100 bp 3'