Canonical Allele Identifier: CA2622960279
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46897125-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897125A>G , CM000675.2:g.46897125A>G GRCh38
NC_000013.10:g.47471260A>G , CM000675.1:g.47471260A>G GRCh37
NC_000013.9:g.46369261A>G NCBI36
NG_013011.1:g.4910T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+827T>C NP_001365853.1:n.-329+827T>C
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