Canonical Allele Identifier: CA955698799
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951102196
gnomAD v3: 13-46896092-G-GT
gnomAD v4: 13-46896092-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896093dup , CM000675.2:g.46896093dup GRCh38
NC_000013.10:g.47470228dup , CM000675.1:g.47470228dup GRCh37
NC_000013.9:g.46368229dup NCBI36
NG_013011.1:g.5942dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-187dup MANE Select ENSP00000437737.1:n.-187dup
ENST00000543956.5:c.-78+581dup ENSP00000441861.2:n.-78+581dup
ENST00000542664.3:c.-187dup ENSP00000437737.1:n.-187dup
ENST00000543956.4:c.160+581dup ENSP00000441861.1:n.160+581dup
NM_000621.4:c.-187dup NP_000612.1:n.-187dup
NM_001165947.2:c.160+581dup NP_001159419.1:n.160+581dup
NM_000621.5:c.-187dup MANE Select NP_000612.1:n.-187dup
NM_001165947.5:c.-78+581dup NP_001159419.2:n.-78+581dup
NM_001378924.1:c.-187dup NP_001365853.1:n.-187dup
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