Canonical Allele Identifier: CA249246211
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs582385

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46871859A>G , CM000675.2:g.46871859A>G GRCh38
NC_000013.10:g.47445994A>G , CM000675.1:g.47445994A>G GRCh37
NC_000013.9:g.46343995A>G NCBI36
NG_013011.1:g.30176T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+20531T>C MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.124+20531T>C ENSP00000441861.2:p.=
ENST00000378688.8:c.613+20531T>C ENSP00000367959.3:p.=
ENST00000542664.3:c.613+20531T>C ENSP00000437737.1:p.=
ENST00000543956.4:c.361+20531T>C ENSP00000441861.1:p.=
NM_000621.4:c.613+20531T>C NP_000612.1:p.=
NM_001165947.2:c.361+20531T>C NP_001159419.1:p.=
NM_000621.5:c.613+20531T>C MANE Select NP_000612.1:p.=
NM_001165947.5:c.124+20531T>C NP_001159419.2:p.=
NM_001378924.1:c.613+20531T>C NP_001365853.1:p.=