Canonical Allele Identifier: CA388154748
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895758T>C , CM000675.2:g.46895758T>C GRCh38
NC_000013.10:g.47469893T>C , CM000675.1:g.47469893T>C GRCh37
NC_000013.9:g.46367894T>C NCBI36
NG_013011.1:g.6277A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.149A>G MANE Select ENSP00000437737.1:p.Glu50Gly
ENST00000543956.5:c.-78+916A>G ENSP00000441861.2:n.-78+916A>G
ENST00000378688.8:c.149A>G ENSP00000367959.3:p.Glu50Gly
ENST00000542664.3:c.149A>G ENSP00000437737.1:p.Glu50Gly
ENST00000543956.4:c.160+916A>G ENSP00000441861.1:n.160+916A>G
ENST00000612998.1:c.56A>G ENSP00000482708.1:p.Glu19Gly
NM_000621.4:c.149A>G NP_000612.1:p.Glu50Gly
NM_001165947.2:c.160+916A>G NP_001159419.1:n.160+916A>G
NM_000621.5:c.149A>G MANE Select NP_000612.1:p.Glu50Gly
NM_001165947.5:c.-78+916A>G NP_001159419.2:n.-78+916A>G
NM_001378924.1:c.149A>G NP_001365853.1:p.Glu50Gly