Canonical Allele Identifier: CA2089308052
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897098A= , CM000675.2:g.46897098A= GRCh38
NC_000013.10:g.47471233A= , CM000675.1:g.47471233A= GRCh37
NC_000013.9:g.46369234A= NCBI36
NG_013011.1:g.4937T=

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+854T= NP_001365853.1:n.-329+854T=