Canonical Allele Identifier: CA2089308230
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs542616894

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897339T>C , CM000675.2:g.46897339T>C GRCh38
NC_000013.10:g.47471474T>C , CM000675.1:g.47471474T>C GRCh37
NC_000013.9:g.46369475T>C NCBI36
NG_013011.1:g.4696A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+613A>G NP_001365853.1:n.-329+613A>G