Canonical Allele Identifier: CA249263501
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs774624231
gnomAD v2: 13-47471376-AAGGT-A
gnomAD v3: 13-46897241-AAGGT-A
gnomAD v4: 13-46897241-AAGGT-A
MyVariant Identifiers: chr13:g.47471377_47471380del (hg19) chr13:g.46897242_46897245del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897247_46897250del , CM000675.2:g.46897247_46897250del GRCh38
NC_000013.10:g.47471382_47471385del , CM000675.1:g.47471382_47471385del GRCh37
NC_000013.9:g.46369383_46369386del NCBI36
NG_013011.1:g.4790_4793del

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+707_-329+710del NP_001365853.1:n.-329+707_-329+710del
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