Canonical Allele Identifier: CA2089297270
Gene: HTR2A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46867680T= , CM000675.2:g.46867680T= GRCh38
NC_000013.10:g.47441815T= , CM000675.1:g.47441815T= GRCh37
NC_000013.9:g.46339816T= NCBI36
NG_013011.1:g.34355A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.613+24710A= MANE Select ENSP00000437737.1:n.613+24710A=
ENST00000543956.5:c.124+24710A= ENSP00000441861.2:n.124+24710A=
ENST00000378688.8:c.613+24710A= ENSP00000367959.3:n.613+24710A=
ENST00000542664.3:c.613+24710A= ENSP00000437737.1:n.613+24710A=
ENST00000543956.4:c.361+24710A= ENSP00000441861.1:n.361+24710A=
NM_000621.4:c.613+24710A= NP_000612.1:n.613+24710A=
NM_001165947.2:c.361+24710A= NP_001159419.1:n.361+24710A=
NM_000621.5:c.613+24710A= MANE Select NP_000612.1:n.613+24710A=
NM_001165947.5:c.124+24710A= NP_001159419.2:n.124+24710A=
NM_001378924.1:c.613+24710A= NP_001365853.1:n.613+24710A=
Search 100 bp 5'
Search 100 bp 3'