Canonical Allele Identifier: CA609569560
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1160114122
gnomAD v2: 13-47471464-G-C
gnomAD v3: 13-46897329-G-C
gnomAD v4: 13-46897329-G-C
MyVariant Identifiers: chr13:g.47471464G>C (hg19) chr13:g.46897329G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897329G>C , CM000675.2:g.46897329G>C GRCh38
NC_000013.10:g.47471464G>C , CM000675.1:g.47471464G>C GRCh37
NC_000013.9:g.46369465G>C NCBI36
NG_013011.1:g.4706C>G

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+623C>G NP_001365853.1:n.-329+623C>G
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