Canonical Allele Identifier: CA388150219
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1378958837

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834886G>A , CM000675.2:g.46834886G>A GRCh38
NC_000013.10:g.47409021G>A , CM000675.1:g.47409021G>A GRCh37
NC_000013.9:g.46307022G>A NCBI36
NG_013011.1:g.67149C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1367C>T MANE Select ENSP00000437737.1:p.Ala456Val
ENST00000543956.5:c.878C>T ENSP00000441861.2:p.Ala293Val
ENST00000378688.8:c.1367C>T ENSP00000367959.3:p.Ala456Val
ENST00000542664.3:c.1367C>T ENSP00000437737.1:p.Ala456Val
ENST00000543956.4:c.1115C>T ENSP00000441861.1:p.Ala372Val
NM_000621.4:c.1367C>T NP_000612.1:p.Ala456Val
NM_001165947.2:c.1115C>T NP_001159419.1:p.Ala372Val
NM_000621.5:c.1367C>T MANE Select NP_000612.1:p.Ala456Val
NM_001165947.5:c.878C>T NP_001159419.2:p.Ala293Val
NM_001378924.1:c.1367C>T NP_001365853.1:p.Ala456Val