Canonical Allele Identifier: CA2089283367
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834921T= , CM000675.2:g.46834921T= GRCh38
NC_000013.10:g.47409056T= , CM000675.1:g.47409056T= GRCh37
NC_000013.9:g.46307057T= NCBI36
NG_013011.1:g.67114A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1332A= MANE Select ENSP00000437737.1:p.Ser444=
ENST00000543956.5:c.843A= ENSP00000441861.2:p.Ser281=
ENST00000378688.8:c.1332A= ENSP00000367959.3:p.Ser444=
ENST00000542664.3:c.1332A= ENSP00000437737.1:p.Ser444=
ENST00000543956.4:c.1080A= ENSP00000441861.1:p.Ser360=
NM_000621.4:c.1332A= NP_000612.1:p.Ser444=
NM_001165947.2:c.1080A= NP_001159419.1:p.Ser360=
NM_000621.5:c.1332A= MANE Select NP_000612.1:p.Ser444=
NM_001165947.5:c.843A= NP_001159419.2:p.Ser281=
NM_001378924.1:c.1332A= NP_001365853.1:p.Ser444=