Canonical Allele Identifier: CA388152849
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1334203728
COSMIC: COSM469475

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46892477C>T , CM000675.2:g.46892477C>T GRCh38
NC_000013.10:g.47466612C>T , CM000675.1:g.47466612C>T GRCh37
NC_000013.9:g.46364613C>T NCBI36
NG_013011.1:g.9558G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.526G>A MANE Select ENSP00000437737.1:p.Ala176Thr
ENST00000543956.5:c.37G>A ENSP00000441861.2:p.Ala13Thr
ENST00000378688.8:c.526G>A ENSP00000367959.3:p.Ala176Thr
ENST00000542664.3:c.526G>A ENSP00000437737.1:p.Ala176Thr
ENST00000543956.4:c.274G>A ENSP00000441861.1:p.Ala92Thr
NM_000621.4:c.526G>A NP_000612.1:p.Ala176Thr
NM_001165947.2:c.274G>A NP_001159419.1:p.Ala92Thr
NM_000621.5:c.526G>A MANE Select NP_000612.1:p.Ala176Thr
NM_001165947.5:c.37G>A NP_001159419.2:p.Ala13Thr
NM_001378924.1:c.526G>A NP_001365853.1:p.Ala176Thr