Canonical Allele Identifier: CA11542871
Gene: HTR3C HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.184060510G>A
GRCh37 chr3:g.183778298G>A
gnomAD v2:
3:183778298 G / A
gnomAD v3:
3:184060510 G / A
gnomAD v4:
chr3-184060510-G-A
Joint Max Group AF 0.7483701 (EAS)
Genomes Max Group AF 0.73159844 (EAS)
Exomes Max Group AF 0.74848038 (EAS)
dbSNP:
6807670
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060510G>A , CM000665.2:g.184060510G>A GRCh38
NC_000003.11:g.183778298G>A , CM000665.1:g.183778298G>A GRCh37
NC_000003.10:g.185260992G>A NCBI36
NG_012749.1:g.12464G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.*158G>A MANE Select ENSP00000322617.1:n.*158G>A
ENST00000318351.1:c.*158G>A ENSP00000322617.1:n.*158G>A
NM_130770.2:c.*158G>A NP_570126.2:n.*158G>A
NM_130770.3:c.*158G>A MANE Select NP_570126.2:n.*158G>A
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