Canonical Allele Identifier: CA609569562
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1381955426

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897366A>C , CM000675.2:g.46897366A>C GRCh38
NC_000013.10:g.47471501A>C , CM000675.1:g.47471501A>C GRCh37
NC_000013.9:g.46369502A>C NCBI36
NG_013011.1:g.4669T>G

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+586T>G NP_001365853.1:n.-329+586T>G