Canonical Allele Identifier: CA2725699
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs181659560
ExAC: 3:183777656 C / G
gnomAD v2: 3-183777656-C-G
gnomAD v3: 3-184059868-C-G
gnomAD v4: 3-184059868-C-G
MyVariant Identifiers: chr3:g.183777656C>G (hg19) chr3:g.184059868C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059868C>G , CM000665.2:g.184059868C>G GRCh38
NC_000003.11:g.183777656C>G , CM000665.1:g.183777656C>G GRCh37
NC_000003.10:g.185260350C>G NCBI36
NG_012749.1:g.11822C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.966C>G MANE Select ENSP00000322617.1:p.Ser322Arg
ENST00000318351.1:c.966C>G ENSP00000322617.1:p.Ser322Arg
NM_130770.2:c.966C>G NP_570126.2:p.Ser322Arg
NM_130770.3:c.966C>G MANE Select NP_570126.2:p.Ser322Arg
Search 100 bp 5'
Search 100 bp 3'