Canonical Allele Identifier: CA2089308170
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951112413

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897290G>C , CM000675.2:g.46897290G>C GRCh38
NC_000013.10:g.47471425G>C , CM000675.1:g.47471425G>C GRCh37
NC_000013.9:g.46369426G>C NCBI36
NG_013011.1:g.4745C>G

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+662C>G NP_001365853.1:n.-329+662C>G