Canonical Allele Identifier: CA2622960238
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46897075-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897075A>G , CM000675.2:g.46897075A>G GRCh38
NC_000013.10:g.47471210A>G , CM000675.1:g.47471210A>G GRCh37
NC_000013.9:g.46369211A>G NCBI36
NG_013011.1:g.4960T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000543956.5:c.-479T>C ENSP00000441861.2:n.-479T>C
ENST00000542664.3:c.-730T>C ENSP00000437737.1:n.-730T>C
ENST00000543956.4:c.-242T>C ENSP00000441861.1:n.-242T>C
NM_000621.4:c.-730T>C NP_000612.1:n.-730T>C
NM_001165947.2:c.-242T>C NP_001159419.1:n.-242T>C
NM_001378924.1:c.-328-841T>C NP_001365853.1:n.-328-841T>C
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