Canonical Allele Identifier: CA15782223
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs3742278

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46845442A>G , CM000675.2:g.46845442A>G GRCh38
NC_000013.10:g.47419577A>G , CM000675.1:g.47419577A>G GRCh37
NC_000013.9:g.46317578A>G NCBI36
NG_013011.1:g.56593T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-9803T>C MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.125-9803T>C ENSP00000441861.2:p.=
ENST00000378688.8:c.614-9803T>C ENSP00000367959.3:p.=
ENST00000542664.3:c.614-9803T>C ENSP00000437737.1:p.=
ENST00000543956.4:c.362-9803T>C ENSP00000441861.1:p.=
NM_000621.4:c.614-9803T>C NP_000612.1:p.=
NM_001165947.2:c.362-9803T>C NP_001159419.1:p.=
NM_000621.5:c.614-9803T>C MANE Select NP_000612.1:p.=
NM_001165947.5:c.125-9803T>C NP_001159419.2:p.=
NM_001378924.1:c.614-9803T>C NP_001365853.1:p.=