Canonical Allele Identifier: CA2622958731
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46834802-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834802G>T , CM000675.2:g.46834802G>T GRCh38
NC_000013.10:g.47408937G>T , CM000675.1:g.47408937G>T GRCh37
NC_000013.9:g.46306938G>T NCBI36
NG_013011.1:g.67233C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.*35C>A MANE Select ENSP00000437737.1:n.*35C>A
ENST00000543956.5:c.*35C>A ENSP00000441861.2:n.*35C>A
ENST00000378688.8:c.*35C>A ENSP00000367959.3:n.*35C>A
ENST00000542664.3:c.*35C>A ENSP00000437737.1:n.*35C>A
ENST00000543956.4:c.*35C>A ENSP00000441861.1:n.*35C>A
NM_000621.4:c.*35C>A NP_000612.1:n.*35C>A
NM_001165947.2:c.*35C>A NP_001159419.1:n.*35C>A
NM_000621.5:c.*35C>A MANE Select NP_000612.1:n.*35C>A
NM_001165947.5:c.*35C>A NP_001159419.2:n.*35C>A
NM_001378924.1:c.*35C>A NP_001365853.1:n.*35C>A
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