Canonical Allele Identifier: CA388153641
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895585C>T , CM000675.2:g.46895585C>T GRCh38
NC_000013.10:g.47469720C>T , CM000675.1:g.47469720C>T GRCh37
NC_000013.9:g.46367721C>T NCBI36
NG_013011.1:g.6450G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.322G>A MANE Select ENSP00000437737.1:p.Ala108Thr
ENST00000543956.5:c.-78+1089G>A ENSP00000441861.2:n.-78+1089G>A
ENST00000378688.8:c.322G>A ENSP00000367959.3:p.Ala108Thr
ENST00000542664.3:c.322G>A ENSP00000437737.1:p.Ala108Thr
ENST00000543956.4:c.160+1089G>A ENSP00000441861.1:n.160+1089G>A
ENST00000612998.1:c.229G>A ENSP00000482708.1:p.Ala77Thr
NM_000621.4:c.322G>A NP_000612.1:p.Ala108Thr
NM_001165947.2:c.160+1089G>A NP_001159419.1:n.160+1089G>A
NM_000621.5:c.322G>A MANE Select NP_000612.1:p.Ala108Thr
NM_001165947.5:c.-78+1089G>A NP_001159419.2:n.-78+1089G>A
NM_001378924.1:c.322G>A NP_001365853.1:p.Ala108Thr