Canonical Allele Identifier: CA2089308073

Gene: HTR2A

Linked Data

• dbSNP Id: rs1814444734

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897120C>G , CM000675.2:g.46897120C>G	GRCh38
NC_000013.10:g.47471255C>G , CM000675.1:g.47471255C>G	GRCh37
NC_000013.9:g.46369256C>G	NCBI36
NG_013011.1:g.4915G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378924.1:c.-329+832G>C	NP_001365853.1:n.-329+832G>C