Canonical Allele Identifier: CA609566058
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1395641718
gnomAD v2: 13-47429450-TCA-T
gnomAD v3: 13-46855315-TCA-T
gnomAD v4: 13-46855315-TCA-T
MyVariant Identifiers: chr13:g.47429451_47429452del (hg19) chr13:g.46855316_46855317del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46855316_46855317del , CM000675.2:g.46855316_46855317del GRCh38
NC_000013.10:g.47429451_47429452del , CM000675.1:g.47429451_47429452del GRCh37
NC_000013.9:g.46327452_46327453del NCBI36
NG_013011.1:g.46718_46719del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-19678_614-19677del (HTR2A) MANE Select ENSP00000437737.1:n.614-19678_614-19677de...
ENST00000543956.5:c.125-19678_125-19677del (HTR2A) ENSP00000441861.2:n.125-19678_125-19677de...
ENST00000378688.8:c.614-19678_614-19677del (HTR2A) ENSP00000367959.3:n.614-19678_614-19677de...
ENST00000542664.3:c.614-19678_614-19677del (HTR2A) ENSP00000437737.1:n.614-19678_614-19677de...
ENST00000543956.4:c.362-19678_362-19677del (HTR2A) ENSP00000441861.1:n.362-19678_362-19677de...
NM_000621.4:c.614-19678_614-19677del (HTR2A) NP_000612.1:n.614-19678_614-19677del
NM_001165947.2:c.362-19678_362-19677del (HTR2A) NP_001159419.1:n.362-19678_362-19677del
NR_046612.1:n.232-774_232-773del (HTR2A-AS1)
NR_103752.1:n.88-774_88-773del (HTR2A-AS1)
NM_000621.5:c.614-19678_614-19677del (HTR2A) MANE Select NP_000612.1:n.614-19678_614-19677del
NM_001165947.5:c.125-19678_125-19677del (HTR2A) NP_001159419.2:n.125-19678_125-19677del
NM_001378924.1:c.614-19678_614-19677del (HTR2A) NP_001365853.1:n.614-19678_614-19677del
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