Canonical Allele Identifier: CA249263474
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs6315
gnomAD v3: 13-46897178-T-G
gnomAD v4: 13-46897178-T-G
MyVariant Identifiers: chr13:g.47471313T>G (hg19) chr13:g.46897178T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897178T>G , CM000675.2:g.46897178T>G GRCh38
NC_000013.10:g.47471313T>G , CM000675.1:g.47471313T>G GRCh37
NC_000013.9:g.46369314T>G NCBI36
NG_013011.1:g.4857A>C

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+774A>C NP_001365853.1:n.-329+774A>C
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