Canonical Allele Identifier: CA609569554
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1260278575
gnomAD v2: 13-47471292-CT-C
gnomAD v3: 13-46897157-CT-C
gnomAD v4: 13-46897157-CT-C
MyVariant Identifiers: chr13:g.47471293del (hg19) chr13:g.46897158del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897162del , CM000675.2:g.46897162del GRCh38
NC_000013.10:g.47471297del , CM000675.1:g.47471297del GRCh37
NC_000013.9:g.46369298del NCBI36
NG_013011.1:g.4877del

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+794del NP_001365853.1:n.-329+794del
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