Canonical Allele Identifier: CA2089283340
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1876380181

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834850dup , CM000675.2:g.46834850dup GRCh38
NC_000013.10:g.47408985dup , CM000675.1:g.47408985dup GRCh37
NC_000013.9:g.46306986dup NCBI36
NG_013011.1:g.67185dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1403dup MANE Select ENSP00000437737.1:p.Ser469GlufsTer7
ENST00000543956.5:c.914dup ENSP00000441861.2:p.Ser306GlufsTer7
ENST00000378688.8:c.1403dup ENSP00000367959.3:p.Ser469GlufsTer7
ENST00000542664.3:c.1403dup ENSP00000437737.1:p.Ser469GlufsTer7
ENST00000543956.4:c.1151dup ENSP00000441861.1:p.Ser385GlufsTer7
NM_000621.4:c.1403dup NP_000612.1:p.Ser469GlufsTer7
NM_001165947.2:c.1151dup NP_001159419.1:p.Ser385GlufsTer7
NM_000621.5:c.1403dup MANE Select NP_000612.1:p.Ser469GlufsTer7
NM_001165947.5:c.914dup NP_001159419.2:p.Ser306GlufsTer7
NM_001378924.1:c.1403dup NP_001365853.1:p.Ser469GlufsTer7