Canonical Allele Identifier: CA2089309136
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1283702466
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46892891dup , CM000675.2:g.46892891dup GRCh38
NC_000013.10:g.47467026dup , CM000675.1:g.47467026dup GRCh37
NC_000013.9:g.46365027dup NCBI36
NG_013011.1:g.9147dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.413-298dup MANE Select ENSP00000437737.1:n.413-298dup
ENST00000543956.5:c.-77-298dup ENSP00000441861.2:n.-77-298dup
ENST00000378688.8:c.413-298dup ENSP00000367959.3:n.413-298dup
ENST00000542664.3:c.413-298dup ENSP00000437737.1:n.413-298dup
ENST00000543956.4:c.161-298dup ENSP00000441861.1:n.161-298dup
NM_000621.4:c.413-298dup NP_000612.1:n.413-298dup
NM_001165947.2:c.161-298dup NP_001159419.1:n.161-298dup
NM_000621.5:c.413-298dup MANE Select NP_000612.1:n.413-298dup
NM_001165947.5:c.-77-298dup NP_001159419.2:n.-77-298dup
NM_001378924.1:c.413-298dup NP_001365853.1:n.413-298dup
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