Canonical Allele Identifier: CA955698950
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951111939

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897168A>T , CM000675.2:g.46897168A>T GRCh38
NC_000013.10:g.47471303A>T , CM000675.1:g.47471303A>T GRCh37
NC_000013.9:g.46369304A>T NCBI36
NG_013011.1:g.4867T>A

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+784T>A NP_001365853.1:n.-329+784T>A