Canonical Allele Identifier: CA13830706
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs3125

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834716C>G , CM000675.2:g.46834716C>G GRCh38
NC_000013.10:g.47408851C>G , CM000675.1:g.47408851C>G GRCh37
NC_000013.9:g.46306852C>G NCBI36
NG_013011.1:g.67319G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.*121G>C MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.*121G>C ENSP00000441861.2:p.=
ENST00000378688.8:c.*121G>C ENSP00000367959.3:p.=
ENST00000542664.3:c.*121G>C ENSP00000437737.1:p.=
ENST00000543956.4:c.*121G>C ENSP00000441861.1:p.=
NM_000621.4:c.*121G>C NP_000612.1:p.=
NM_001165947.2:c.*121G>C NP_001159419.1:p.=
NM_000621.5:c.*121G>C MANE Select NP_000612.1:p.=
NM_001165947.5:c.*121G>C NP_001159419.2:p.=
NM_001378924.1:c.*121G>C NP_001365853.1:p.=