Canonical Allele Identifier: CA698547233
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1252123082

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897365_46897367del , CM000675.2:g.46897365_46897367del GRCh38
NC_000013.10:g.47471500_47471502del , CM000675.1:g.47471500_47471502del GRCh37
NC_000013.9:g.46369501_46369503del NCBI36
NG_013011.1:g.4668_4670del

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+585_-329+587del NP_001365853.1:n.-329+585_-329+587del