Canonical Allele Identifier: CA955698954
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951111993

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897173A>G , CM000675.2:g.46897173A>G GRCh38
NC_000013.10:g.47471308A>G , CM000675.1:g.47471308A>G GRCh37
NC_000013.9:g.46369309A>G NCBI36
NG_013011.1:g.4862T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+779T>C NP_001365853.1:n.-329+779T>C