Canonical Allele Identifier: CA609929154
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs886289270
gnomAD v2: 13-47408900-A-AT
gnomAD v3: 13-46834765-A-AT
gnomAD v4: 13-46834765-A-AT
MyVariant Identifiers: chr13:g.47408900_47408901insT (hg19) chr13:g.46834765_46834766insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834766dup , CM000675.2:g.46834766dup GRCh38
NC_000013.10:g.47408901dup , CM000675.1:g.47408901dup GRCh37
NC_000013.9:g.46306902dup NCBI36
NG_013011.1:g.67269dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.*71dup MANE Select ENSP00000437737.1:n.*71dup
ENST00000543956.5:c.*71dup ENSP00000441861.2:n.*71dup
ENST00000378688.8:c.*71dup ENSP00000367959.3:n.*71dup
ENST00000542664.3:c.*71dup ENSP00000437737.1:n.*71dup
ENST00000543956.4:c.*71dup ENSP00000441861.1:n.*71dup
NM_000621.4:c.*71dup NP_000612.1:n.*71dup
NM_001165947.2:c.*71dup NP_001159419.1:n.*71dup
NM_000621.5:c.*71dup MANE Select NP_000612.1:n.*71dup
NM_001165947.5:c.*71dup NP_001159419.2:n.*71dup
NM_001378924.1:c.*71dup NP_001365853.1:n.*71dup
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