Canonical Allele Identifier: CA2089308265
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951112857

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897359A>T , CM000675.2:g.46897359A>T GRCh38
NC_000013.10:g.47471494A>T , CM000675.1:g.47471494A>T GRCh37
NC_000013.9:g.46369495A>T NCBI36
NG_013011.1:g.4676T>A

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+593T>A NP_001365853.1:n.-329+593T>A