Canonical Allele Identifier: CA698547215
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1326345468
gnomAD v3: 13-46897319-T-C
gnomAD v4: 13-46897319-T-C
MyVariant Identifiers: chr13:g.47471454T>C (hg19) chr13:g.46897319T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897319T>C , CM000675.2:g.46897319T>C GRCh38
NC_000013.10:g.47471454T>C , CM000675.1:g.47471454T>C GRCh37
NC_000013.9:g.46369455T>C NCBI36
NG_013011.1:g.4716A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+633A>G NP_001365853.1:n.-329+633A>G
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