Canonical Allele Identifier: CA388150452
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834949T>A , CM000675.2:g.46834949T>A GRCh38
NC_000013.10:g.47409084T>A , CM000675.1:g.47409084T>A GRCh37
NC_000013.9:g.46307085T>A NCBI36
NG_013011.1:g.67086A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1304A>T MANE Select ENSP00000437737.1:p.Asp435Val
ENST00000543956.5:c.815A>T ENSP00000441861.2:p.Asp272Val
ENST00000378688.8:c.1304A>T ENSP00000367959.3:p.Asp435Val
ENST00000542664.3:c.1304A>T ENSP00000437737.1:p.Asp435Val
ENST00000543956.4:c.1052A>T ENSP00000441861.1:p.Asp351Val
NM_000621.4:c.1304A>T NP_000612.1:p.Asp435Val
NM_001165947.2:c.1052A>T NP_001159419.1:p.Asp351Val
NM_000621.5:c.1304A>T MANE Select NP_000612.1:p.Asp435Val
NM_001165947.5:c.815A>T NP_001159419.2:p.Asp272Val
NM_001378924.1:c.1304A>T NP_001365853.1:p.Asp435Val