Canonical Allele Identifier: CA2089283361
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834905T= , CM000675.2:g.46834905T= GRCh38
NC_000013.10:g.47409040T= , CM000675.1:g.47409040T= GRCh37
NC_000013.9:g.46307041T= NCBI36
NG_013011.1:g.67130A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1348A= MANE Select ENSP00000437737.1:p.Lys450=
ENST00000543956.5:c.859A= ENSP00000441861.2:p.Lys287=
ENST00000378688.8:c.1348A= ENSP00000367959.3:p.Lys450=
ENST00000542664.3:c.1348A= ENSP00000437737.1:p.Lys450=
ENST00000543956.4:c.1096A= ENSP00000441861.1:p.Lys366=
NM_000621.4:c.1348A= NP_000612.1:p.Lys450=
NM_001165947.2:c.1096A= NP_001159419.1:p.Lys366=
NM_000621.5:c.1348A= MANE Select NP_000612.1:p.Lys450=
NM_001165947.5:c.859A= NP_001159419.2:p.Lys287=
NM_001378924.1:c.1348A= NP_001365853.1:p.Lys450=