Canonical Allele Identifier: CA2089297231
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1950827846
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46867601del , CM000675.2:g.46867601del GRCh38
NC_000013.10:g.47441736del , CM000675.1:g.47441736del GRCh37
NC_000013.9:g.46339737del NCBI36
NG_013011.1:g.34434del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+24789del MANE Select ENSP00000437737.1:n.613+24789del
ENST00000543956.5:c.124+24789del ENSP00000441861.2:n.124+24789del
ENST00000378688.8:c.613+24789del ENSP00000367959.3:n.613+24789del
ENST00000542664.3:c.613+24789del ENSP00000437737.1:n.613+24789del
ENST00000543956.4:c.361+24789del ENSP00000441861.1:n.361+24789del
NM_000621.4:c.613+24789del NP_000612.1:n.613+24789del
NM_001165947.2:c.361+24789del NP_001159419.1:n.361+24789del
NM_000621.5:c.613+24789del MANE Select NP_000612.1:n.613+24789del
NM_001165947.5:c.124+24789del NP_001159419.2:n.124+24789del
NM_001378924.1:c.613+24789del NP_001365853.1:n.613+24789del
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