Canonical Allele Identifier: CA483739026
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs58145637
gnomAD v2: 13-47408902-A-ATT
gnomAD v3: 13-46834767-A-ATT
gnomAD v4: 13-46834767-A-ATT
MyVariant Identifiers: chr13:g.47408903_47408904insTT (hg19) chr13:g.47408902_47408903insTT (hg19) chr13:g.46834768_46834769insTT (hg38) chr13:g.46834767_46834768insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834777_46834778dup , CM000675.2:g.46834777_46834778dup GRCh38
NC_000013.10:g.47408912_47408913dup , CM000675.1:g.47408912_47408913dup GRCh37
NC_000013.9:g.46306913_46306914dup NCBI36
NG_013011.1:g.67266_67267dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.*68_*69dup MANE Select ENSP00000437737.1:n.*68_*69dup
ENST00000543956.5:c.*68_*69dup ENSP00000441861.2:n.*68_*69dup
ENST00000378688.8:c.*68_*69dup ENSP00000367959.3:n.*68_*69dup
ENST00000542664.3:c.*68_*69dup ENSP00000437737.1:n.*68_*69dup
ENST00000543956.4:c.*68_*69dup ENSP00000441861.1:n.*68_*69dup
NM_000621.4:c.*68_*69dup NP_000612.1:n.*68_*69dup
NM_001165947.2:c.*68_*69dup NP_001159419.1:n.*68_*69dup
NM_000621.5:c.*68_*69dup MANE Select NP_000612.1:n.*68_*69dup
NM_001165947.5:c.*68_*69dup NP_001159419.2:n.*68_*69dup
NM_001378924.1:c.*68_*69dup NP_001365853.1:n.*68_*69dup
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