Canonical Allele Identifier: CA2622960237
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897074C>T , CM000675.2:g.46897074C>T GRCh38
NC_000013.10:g.47471209C>T , CM000675.1:g.47471209C>T GRCh37
NC_000013.9:g.46369210C>T NCBI36
NG_013011.1:g.4961G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000543956.5:c.-478G>A ENSP00000441861.2:n.-478G>A
ENST00000542664.3:c.-729G>A ENSP00000437737.1:n.-729G>A
ENST00000543956.4:c.-241G>A ENSP00000441861.1:n.-241G>A
NM_000621.4:c.-729G>A NP_000612.1:n.-729G>A
NM_001165947.2:c.-241G>A NP_001159419.1:n.-241G>A
NM_001378924.1:c.-328-840G>A NP_001365853.1:n.-328-840G>A