Canonical Allele Identifier: CA437322943
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1723411931
gnomAD v4: 3-184059967-C-T
MyVariant Identifiers: chr3:g.183777755C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059967C>T , CM000665.2:g.184059967C>T GRCh38
NC_000003.11:g.183777755C>T , CM000665.1:g.183777755C>T GRCh37
NC_000003.10:g.185260449C>T NCBI36
NG_012749.1:g.11921C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1065C>T MANE Select ENSP00000322617.1:p.Thr355=
ENST00000318351.1:c.1065C>T ENSP00000322617.1:p.Thr355=
NM_130770.2:c.1065C>T NP_570126.2:p.Thr355=
NM_130770.3:c.1065C>T MANE Select NP_570126.2:p.Thr355=
Search 100 bp 5'
Search 100 bp 3'