Canonical Allele Identifier: CA2089308017
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897066C= , CM000675.2:g.46897066C= GRCh38
NC_000013.10:g.47471201C= , CM000675.1:g.47471201C= GRCh37
NC_000013.9:g.46369202C= NCBI36
NG_013011.1:g.4969G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543956.5:c.-470G= ENSP00000441861.2:n.-470G=
ENST00000542664.3:c.-721G= ENSP00000437737.1:n.-721G=
ENST00000543956.4:c.-233G= ENSP00000441861.1:n.-233G=
NM_000621.4:c.-721G= NP_000612.1:n.-721G=
NM_001165947.2:c.-233G= NP_001159419.1:n.-233G=
NM_001378924.1:c.-328-832G= NP_001365853.1:n.-328-832G=