Canonical Allele Identifier: CA2089283409
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835021A= , CM000675.2:g.46835021A= GRCh38
NC_000013.10:g.47409156A= , CM000675.1:g.47409156A= GRCh37
NC_000013.9:g.46307157A= NCBI36
NG_013011.1:g.67014T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1232T= MANE Select ENSP00000437737.1:p.Val411=
ENST00000543956.5:c.743T= ENSP00000441861.2:p.Val248=
ENST00000378688.8:c.1232T= ENSP00000367959.3:p.Val411=
ENST00000542664.3:c.1232T= ENSP00000437737.1:p.Val411=
ENST00000543956.4:c.980T= ENSP00000441861.1:p.Val327=
NM_000621.4:c.1232T= NP_000612.1:p.Val411=
NM_001165947.2:c.980T= NP_001159419.1:p.Val327=
NM_000621.5:c.1232T= MANE Select NP_000612.1:p.Val411=
NM_001165947.5:c.743T= NP_001159419.2:p.Val248=
NM_001378924.1:c.1232T= NP_001365853.1:p.Val411=