Canonical Allele Identifier: CA698547122
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1292850151
gnomAD v3: 13-46897204-G-T
gnomAD v4: 13-46897204-G-T
MyVariant Identifiers: chr13:g.47471339G>T (hg19) chr13:g.46897204G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897204G>T , CM000675.2:g.46897204G>T GRCh38
NC_000013.10:g.47471339G>T , CM000675.1:g.47471339G>T GRCh37
NC_000013.9:g.46369340G>T NCBI36
NG_013011.1:g.4831C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+748C>A NP_001365853.1:n.-329+748C>A
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