Canonical Allele Identifier: CA698547244
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1194069380

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897368T>A , CM000675.2:g.46897368T>A GRCh38
NC_000013.10:g.47471503T>A , CM000675.1:g.47471503T>A GRCh37
NC_000013.9:g.46369504T>A NCBI36
NG_013011.1:g.4667A>T

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+584A>T NP_001365853.1:n.-329+584A>T