Canonical Allele Identifier: CA2089304487
Gene: HTR2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46884006T= , CM000675.2:g.46884006T= GRCh38
NC_000013.10:g.47458141T= , CM000675.1:g.47458141T= GRCh37
NC_000013.9:g.46356142T= NCBI36
NG_013011.1:g.18029A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.613+8384A= MANE Select ENSP00000437737.1:n.613+8384A=
ENST00000543956.5:c.124+8384A= ENSP00000441861.2:n.124+8384A=
ENST00000378688.8:c.613+8384A= ENSP00000367959.3:n.613+8384A=
ENST00000542664.3:c.613+8384A= ENSP00000437737.1:n.613+8384A=
ENST00000543956.4:c.361+8384A= ENSP00000441861.1:n.361+8384A=
NM_000621.4:c.613+8384A= NP_000612.1:n.613+8384A=
NM_001165947.2:c.361+8384A= NP_001159419.1:n.361+8384A=
NM_000621.5:c.613+8384A= MANE Select NP_000612.1:n.613+8384A=
NM_001165947.5:c.124+8384A= NP_001159419.2:n.124+8384A=
NM_001378924.1:c.613+8384A= NP_001365853.1:n.613+8384A=
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