Canonical Allele Identifier: CA2089308192
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897314C= , CM000675.2:g.46897314C= GRCh38
NC_000013.10:g.47471449C= , CM000675.1:g.47471449C= GRCh37
NC_000013.9:g.46369450C= NCBI36
NG_013011.1:g.4721G=

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+638G= NP_001365853.1:n.-329+638G=