Canonical Allele Identifier: CA13830706
Gene: HTR2A HGNC NCBI
MyVariant.info:
GRCh38 chr13:g.46834716C>G
GRCh37 chr13:g.47408851C>G
gnomAD v2:
13:47408851 C / G
gnomAD v3:
13:46834716 C / G
gnomAD v4:
chr13-46834716-C-G
Joint Max Group AF 0.20379443 (EAS)
Genomes Max Group AF 0.18203995 (AMR)
Exomes Max Group AF 0.2089007 (AMR)
dbSNP:
3125
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834716C>G , CM000675.2:g.46834716C>G GRCh38
NC_000013.10:g.47408851C>G , CM000675.1:g.47408851C>G GRCh37
NC_000013.9:g.46306852C>G NCBI36
NG_013011.1:g.67319G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.*121G>C MANE Select ENSP00000437737.1:n.*121G>C
ENST00000543956.5:c.*121G>C ENSP00000441861.2:n.*121G>C
ENST00000378688.8:c.*121G>C ENSP00000367959.3:n.*121G>C
ENST00000542664.3:c.*121G>C ENSP00000437737.1:n.*121G>C
ENST00000543956.4:c.*121G>C ENSP00000441861.1:n.*121G>C
NM_000621.4:c.*121G>C NP_000612.1:n.*121G>C
NM_001165947.2:c.*121G>C NP_001159419.1:n.*121G>C
NM_000621.5:c.*121G>C MANE Select NP_000612.1:n.*121G>C
NM_001165947.5:c.*121G>C NP_001159419.2:n.*121G>C
NM_001378924.1:c.*121G>C NP_001365853.1:n.*121G>C
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