Canonical Allele Identifier: CA249263534
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs966173282
gnomAD v3: 13-46897323-C-T
gnomAD v4: 13-46897323-C-T
MyVariant Identifiers: chr13:g.47471458C>T (hg19) chr13:g.46897323C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897323C>T , CM000675.2:g.46897323C>T GRCh38
NC_000013.10:g.47471458C>T , CM000675.1:g.47471458C>T GRCh37
NC_000013.9:g.46369459C>T NCBI36
NG_013011.1:g.4712G>A

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+629G>A NP_001365853.1:n.-329+629G>A
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