Canonical Allele Identifier: CA2592686379
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2138262102

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897104T>C , CM000675.2:g.46897104T>C GRCh38
NC_000013.10:g.47471239T>C , CM000675.1:g.47471239T>C GRCh37
NC_000013.9:g.46369240T>C NCBI36
NG_013011.1:g.4931A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+848A>G NP_001365853.1:n.-329+848A>G