Canonical Allele Identifier: CA355378814
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1404935077
gnomAD v2: 3-183777748-A-T
gnomAD v4: 3-184059960-A-T
COSMIC: COSM3373106
MyVariant Identifiers: chr3:g.183777748A>T (hg19) chr3:g.184059960A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059960A>T , CM000665.2:g.184059960A>T GRCh38
NC_000003.11:g.183777748A>T , CM000665.1:g.183777748A>T GRCh37
NC_000003.10:g.185260442A>T NCBI36
NG_012749.1:g.11914A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1058A>T MANE Select ENSP00000322617.1:p.His353Leu
ENST00000318351.1:c.1058A>T ENSP00000322617.1:p.His353Leu
NM_130770.2:c.1058A>T NP_570126.2:p.His353Leu
NM_130770.3:c.1058A>T MANE Select NP_570126.2:p.His353Leu
Search 100 bp 5'
Search 100 bp 3'