Canonical Allele Identifier: CA2089283347
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834867G= , CM000675.2:g.46834867G= GRCh38
NC_000013.10:g.47409002G= , CM000675.1:g.47409002G= GRCh37
NC_000013.9:g.46307003G= NCBI36
NG_013011.1:g.67168C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1386C= MANE Select ENSP00000437737.1:p.Asp462=
ENST00000543956.5:c.897C= ENSP00000441861.2:p.Asp299=
ENST00000378688.8:c.1386C= ENSP00000367959.3:p.Asp462=
ENST00000542664.3:c.1386C= ENSP00000437737.1:p.Asp462=
ENST00000543956.4:c.1134C= ENSP00000441861.1:p.Asp378=
NM_000621.4:c.1386C= NP_000612.1:p.Asp462=
NM_001165947.2:c.1134C= NP_001159419.1:p.Asp378=
NM_000621.5:c.1386C= MANE Select NP_000612.1:p.Asp462=
NM_001165947.5:c.897C= NP_001159419.2:p.Asp299=
NM_001378924.1:c.1386C= NP_001365853.1:p.Asp462=