Canonical Allele Identifier: CA2089308251
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951112800

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897350T>G , CM000675.2:g.46897350T>G GRCh38
NC_000013.10:g.47471485T>G , CM000675.1:g.47471485T>G GRCh37
NC_000013.9:g.46369486T>G NCBI36
NG_013011.1:g.4685A>C

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+602A>C NP_001365853.1:n.-329+602A>C