Canonical Allele Identifier: CA2089308092
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897168A= , CM000675.2:g.46897168A= GRCh38
NC_000013.10:g.47471303A= , CM000675.1:g.47471303A= GRCh37
NC_000013.9:g.46369304A= NCBI36
NG_013011.1:g.4867T=

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+784T= NP_001365853.1:n.-329+784T=