Canonical Allele Identifier: CA388150329
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834916A>T , CM000675.2:g.46834916A>T GRCh38
NC_000013.10:g.47409051A>T , CM000675.1:g.47409051A>T GRCh37
NC_000013.9:g.46307052A>T NCBI36
NG_013011.1:g.67119T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1337T>A MANE Select ENSP00000437737.1:p.Val446Asp
ENST00000543956.5:c.848T>A ENSP00000441861.2:p.Val283Asp
ENST00000378688.8:c.1337T>A ENSP00000367959.3:p.Val446Asp
ENST00000542664.3:c.1337T>A ENSP00000437737.1:p.Val446Asp
ENST00000543956.4:c.1085T>A ENSP00000441861.1:p.Val362Asp
NM_000621.4:c.1337T>A NP_000612.1:p.Val446Asp
NM_001165947.2:c.1085T>A NP_001159419.1:p.Val362Asp
NM_000621.5:c.1337T>A MANE Select NP_000612.1:p.Val446Asp
NM_001165947.5:c.848T>A NP_001159419.2:p.Val283Asp
NM_001378924.1:c.1337T>A NP_001365853.1:p.Val446Asp