Canonical Allele Identifier: CA2089309005
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1593446691
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46892758A>G , CM000675.2:g.46892758A>G GRCh38
NC_000013.10:g.47466893A>G , CM000675.1:g.47466893A>G GRCh37
NC_000013.9:g.46364894A>G NCBI36
NG_013011.1:g.9277T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.413-168T>C MANE Select ENSP00000437737.1:n.413-168T>C
ENST00000543956.5:c.-77-168T>C ENSP00000441861.2:n.-77-168T>C
ENST00000378688.8:c.413-168T>C ENSP00000367959.3:n.413-168T>C
ENST00000542664.3:c.413-168T>C ENSP00000437737.1:n.413-168T>C
ENST00000543956.4:c.161-168T>C ENSP00000441861.1:n.161-168T>C
NM_000621.4:c.413-168T>C NP_000612.1:n.413-168T>C
NM_001165947.2:c.161-168T>C NP_001159419.1:n.161-168T>C
NM_000621.5:c.413-168T>C MANE Select NP_000612.1:n.413-168T>C
NM_001165947.5:c.-77-168T>C NP_001159419.2:n.-77-168T>C
NM_001378924.1:c.413-168T>C NP_001365853.1:n.413-168T>C
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