Canonical Allele Identifier: CA2622960292
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46897143-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897143T>G , CM000675.2:g.46897143T>G GRCh38
NC_000013.10:g.47471278T>G , CM000675.1:g.47471278T>G GRCh37
NC_000013.9:g.46369279T>G NCBI36
NG_013011.1:g.4892A>C

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+809A>C NP_001365853.1:n.-329+809A>C
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Search 100 bp 3'