Canonical Allele Identifier: CA2089292896
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46855318G= , CM000675.2:g.46855318G= GRCh38
NC_000013.10:g.47429453G= , CM000675.1:g.47429453G= GRCh37
NC_000013.9:g.46327454G= NCBI36
NG_013011.1:g.46717C=

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-19679C= (HTR2A) MANE Select ENSP00000437737.1:n.614-19679C=
ENST00000543956.5:c.125-19679C= (HTR2A) ENSP00000441861.2:n.125-19679C=
ENST00000378688.8:c.614-19679C= (HTR2A) ENSP00000367959.3:n.614-19679C=
ENST00000542664.3:c.614-19679C= (HTR2A) ENSP00000437737.1:n.614-19679C=
ENST00000543956.4:c.362-19679C= (HTR2A) ENSP00000441861.1:n.362-19679C=
NM_000621.4:c.614-19679C= (HTR2A) NP_000612.1:n.614-19679C=
NM_001165947.2:c.362-19679C= (HTR2A) NP_001159419.1:n.362-19679C=
NR_046612.1:n.232-772G= (HTR2A-AS1)
NR_103752.1:n.88-772G= (HTR2A-AS1)
NM_000621.5:c.614-19679C= (HTR2A) MANE Select NP_000612.1:n.614-19679C=
NM_001165947.5:c.125-19679C= (HTR2A) NP_001159419.2:n.125-19679C=
NM_001378924.1:c.614-19679C= (HTR2A) NP_001365853.1:n.614-19679C=