Canonical Allele Identifier: CA2089311426
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895719G= , CM000675.2:g.46895719G= GRCh38
NC_000013.10:g.47469854G= , CM000675.1:g.47469854G= GRCh37
NC_000013.9:g.46367855G= NCBI36
NG_013011.1:g.6316C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.188C= MANE Select ENSP00000437737.1:p.Pro63=
ENST00000543956.5:c.-78+955C= ENSP00000441861.2:n.-78+955C=
ENST00000378688.8:c.188C= ENSP00000367959.3:p.Pro63=
ENST00000542664.3:c.188C= ENSP00000437737.1:p.Pro63=
ENST00000543956.4:c.160+955C= ENSP00000441861.1:n.160+955C=
ENST00000612998.1:c.95C= ENSP00000482708.1:p.Pro32=
NM_000621.4:c.188C= NP_000612.1:p.Pro63=
NM_001165947.2:c.160+955C= NP_001159419.1:n.160+955C=
NM_000621.5:c.188C= MANE Select NP_000612.1:p.Pro63=
NM_001165947.5:c.-78+955C= NP_001159419.2:n.-78+955C=
NM_001378924.1:c.188C= NP_001365853.1:p.Pro63=