Canonical Allele Identifier: CA609929155
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs58145637
gnomAD v2: 13-47408902-AT-A
gnomAD v3: 13-46834767-AT-A
gnomAD v4: 13-46834767-AT-A
COSMIC: COSN1158956
MyVariant Identifiers: chr13:g.47408903del (hg19) chr13:g.46834768del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834778del , CM000675.2:g.46834778del GRCh38
NC_000013.10:g.47408913del , CM000675.1:g.47408913del GRCh37
NC_000013.9:g.46306914del NCBI36
NG_013011.1:g.67267del

Transcript Alleles

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