Canonical Allele Identifier: CA2089283702
Gene: HTR2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835866A= , CM000675.2:g.46835866A= GRCh38
NC_000013.10:g.47410001A= , CM000675.1:g.47410001A= GRCh37
NC_000013.9:g.46308002A= NCBI36
NG_013011.1:g.66169T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.614-227T= MANE Select ENSP00000437737.1:n.614-227T=
ENST00000543956.5:c.125-227T= ENSP00000441861.2:n.125-227T=
ENST00000378688.8:c.614-227T= ENSP00000367959.3:n.614-227T=
ENST00000542664.3:c.614-227T= ENSP00000437737.1:n.614-227T=
ENST00000543956.4:c.362-227T= ENSP00000441861.1:n.362-227T=
NM_000621.4:c.614-227T= NP_000612.1:n.614-227T=
NM_001165947.2:c.362-227T= NP_001159419.1:n.362-227T=
NM_000621.5:c.614-227T= MANE Select NP_000612.1:n.614-227T=
NM_001165947.5:c.125-227T= NP_001159419.2:n.125-227T=
NM_001378924.1:c.614-227T= NP_001365853.1:n.614-227T=
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