Canonical Allele Identifier: CA2622959682
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46896018-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896019dup , CM000675.2:g.46896019dup GRCh38
NC_000013.10:g.47470154dup , CM000675.1:g.47470154dup GRCh37
NC_000013.9:g.46368155dup NCBI36
NG_013011.1:g.6016dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-113dup MANE Select ENSP00000437737.1:n.-113dup
ENST00000543956.5:c.-78+655dup ENSP00000441861.2:n.-78+655dup
ENST00000378688.8:c.-113dup ENSP00000367959.3:n.-113dup
ENST00000542664.3:c.-113dup ENSP00000437737.1:n.-113dup
ENST00000543956.4:c.160+655dup ENSP00000441861.1:n.160+655dup
NM_000621.4:c.-113dup NP_000612.1:n.-113dup
NM_001165947.2:c.160+655dup NP_001159419.1:n.160+655dup
NM_000621.5:c.-113dup MANE Select NP_000612.1:n.-113dup
NM_001165947.5:c.-78+655dup NP_001159419.2:n.-78+655dup
NM_001378924.1:c.-113dup NP_001365853.1:n.-113dup
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