Canonical Allele Identifier: CA609566064
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1228867177
gnomAD v2: 13-47429468-CAT-C
gnomAD v3: 13-46855333-CAT-C
gnomAD v4: 13-46855333-CAT-C
MyVariant Identifiers: chr13:g.47429469_47429470del (hg19) chr13:g.46855334_46855335del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46855334_46855335del , CM000675.2:g.46855334_46855335del GRCh38
NC_000013.10:g.47429469_47429470del , CM000675.1:g.47429469_47429470del GRCh37
NC_000013.9:g.46327470_46327471del NCBI36
NG_013011.1:g.46700_46701del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-19696_614-19695del (HTR2A) MANE Select ENSP00000437737.1:n.614-19696_614-19695de...
ENST00000543956.5:c.125-19696_125-19695del (HTR2A) ENSP00000441861.2:n.125-19696_125-19695de...
ENST00000378688.8:c.614-19696_614-19695del (HTR2A) ENSP00000367959.3:n.614-19696_614-19695de...
ENST00000542664.3:c.614-19696_614-19695del (HTR2A) ENSP00000437737.1:n.614-19696_614-19695de...
ENST00000543956.4:c.362-19696_362-19695del (HTR2A) ENSP00000441861.1:n.362-19696_362-19695de...
NM_000621.4:c.614-19696_614-19695del (HTR2A) NP_000612.1:n.614-19696_614-19695del
NM_001165947.2:c.362-19696_362-19695del (HTR2A) NP_001159419.1:n.362-19696_362-19695del
NR_046612.1:n.232-756_232-755del (HTR2A-AS1)
NR_103752.1:n.88-756_88-755del (HTR2A-AS1)
NM_000621.5:c.614-19696_614-19695del (HTR2A) MANE Select NP_000612.1:n.614-19696_614-19695del
NM_001165947.5:c.125-19696_125-19695del (HTR2A) NP_001159419.2:n.125-19696_125-19695del
NM_001378924.1:c.614-19696_614-19695del (HTR2A) NP_001365853.1:n.614-19696_614-19695del
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