Canonical Allele Identifier: CA6284376
Gene: HTR3A HGNC NCBI
gnomAD v2:
11:113848273 A / T
gnomAD v3:
11:113977551 A / T
gnomAD v4:
chr11-113977551-A-T
Joint Max Group AF 0.68930409 (SAS)
Genomes Max Group AF 0.66943225 (NFE)
Exomes Max Group AF 0.6896953 (SAS)
dbSNP:
1985242
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113977551A>T , CM000673.2:g.113977551A>T GRCh38
NC_000011.9:g.113848273A>T , CM000673.1:g.113848273A>T GRCh37
NC_000011.8:g.113353483A>T NCBI36
NG_013058.1:g.7477A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504030.7:c.68-220A>T MANE Select ENSP00000424189.2:n.68-220A>T
ENST00000299961.5:c.-4A>T ENSP00000299961.4:n.-4A>T
ENST00000355556.6:c.86-220A>T ENSP00000347754.2:n.86-220A>T
ENST00000375498.6:c.86-220A>T ENSP00000364648.2:n.86-220A>T
ENST00000504030.6:c.68-220A>T ENSP00000424189.2:n.68-220A>T
ENST00000506841.6:c.68-220A>T ENSP00000424776.2:n.68-220A>T
ENST00000510849.5:c.68-220A>T ENSP00000423653.1:n.68-220A>T
NM_000869.5:c.86-220A>T NP_000860.2:n.86-220A>T
NM_001161772.2:c.-4A>T NP_001155244.1:n.-4A>T
NM_213621.3:c.86-220A>T NP_998786.2:n.86-220A>T
NR_046363.1:n.319-220A>T
NM_000869.6:c.68-220A>T MANE Select NP_000860.3:n.68-220A>T
NM_213621.4:c.68-220A>T NP_998786.3:n.68-220A>T
NM_001161772.3:c.-4A>T NP_001155244.1:n.-4A>T
NR_046363.2:n.286-220A>T
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