Canonical Allele Identifier: CA955698947
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951111826
gnomAD v4: 13-46897134-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897134C>A , CM000675.2:g.46897134C>A GRCh38
NC_000013.10:g.47471269C>A , CM000675.1:g.47471269C>A GRCh37
NC_000013.9:g.46369270C>A NCBI36
NG_013011.1:g.4901G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+818G>T NP_001365853.1:n.-329+818G>T
Search 100 bp 5'
Search 100 bp 3'