Canonical Allele Identifier: CA355379442
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1319092577
gnomAD v2: 3-183777983-G-C
gnomAD v3: 3-184060195-G-C
gnomAD v4: 3-184060195-G-C
COSMIC: COSM729606
MyVariant Identifiers: chr3:g.183777983G>C (hg19) chr3:g.184060195G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060195G>C , CM000665.2:g.184060195G>C GRCh38
NC_000003.11:g.183777983G>C , CM000665.1:g.183777983G>C GRCh37
NC_000003.10:g.185260677G>C NCBI36
NG_012749.1:g.12149G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1187G>C MANE Select ENSP00000322617.1:p.Arg396Thr
ENST00000318351.1:c.1187G>C ENSP00000322617.1:p.Arg396Thr
NM_130770.2:c.1187G>C NP_570126.2:p.Arg396Thr
NM_130770.3:c.1187G>C MANE Select NP_570126.2:p.Arg396Thr
Search 100 bp 5'
Search 100 bp 3'