Canonical Allele Identifier: CA388150558
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834973C>A , CM000675.2:g.46834973C>A GRCh38
NC_000013.10:g.47409108C>A , CM000675.1:g.47409108C>A GRCh37
NC_000013.9:g.46307109C>A NCBI36
NG_013011.1:g.67062G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1280G>T MANE Select ENSP00000437737.1:p.Gly427Val
ENST00000543956.5:c.791G>T ENSP00000441861.2:p.Gly264Val
ENST00000378688.8:c.1280G>T ENSP00000367959.3:p.Gly427Val
ENST00000542664.3:c.1280G>T ENSP00000437737.1:p.Gly427Val
ENST00000543956.4:c.1028G>T ENSP00000441861.1:p.Gly343Val
NM_000621.4:c.1280G>T NP_000612.1:p.Gly427Val
NM_001165947.2:c.1028G>T NP_001159419.1:p.Gly343Val
NM_000621.5:c.1280G>T MANE Select NP_000612.1:p.Gly427Val
NM_001165947.5:c.791G>T NP_001159419.2:p.Gly264Val
NM_001378924.1:c.1280G>T NP_001365853.1:p.Gly427Val