Canonical Allele Identifier: CA2089283370
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834928T= , CM000675.2:g.46834928T= GRCh38
NC_000013.10:g.47409063T= , CM000675.1:g.47409063T= GRCh37
NC_000013.9:g.46307064T= NCBI36
NG_013011.1:g.67107A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1325A= MANE Select ENSP00000437737.1:p.Asp442=
ENST00000543956.5:c.836A= ENSP00000441861.2:p.Asp279=
ENST00000378688.8:c.1325A= ENSP00000367959.3:p.Asp442=
ENST00000542664.3:c.1325A= ENSP00000437737.1:p.Asp442=
ENST00000543956.4:c.1073A= ENSP00000441861.1:p.Asp358=
NM_000621.4:c.1325A= NP_000612.1:p.Asp442=
NM_001165947.2:c.1073A= NP_001159419.1:p.Asp358=
NM_000621.5:c.1325A= MANE Select NP_000612.1:p.Asp442=
NM_001165947.5:c.836A= NP_001159419.2:p.Asp279=
NM_001378924.1:c.1325A= NP_001365853.1:p.Asp442=