Canonical Allele Identifier: CA955698794
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951102012
gnomAD v3: 13-46896072-A-T
gnomAD v4: 13-46896072-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896072A>T , CM000675.2:g.46896072A>T GRCh38
NC_000013.10:g.47470207A>T , CM000675.1:g.47470207A>T GRCh37
NC_000013.9:g.46368208A>T NCBI36
NG_013011.1:g.5963T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-166T>A MANE Select ENSP00000437737.1:n.-166T>A
ENST00000543956.5:c.-78+602T>A ENSP00000441861.2:n.-78+602T>A
ENST00000542664.3:c.-166T>A ENSP00000437737.1:n.-166T>A
ENST00000543956.4:c.160+602T>A ENSP00000441861.1:n.160+602T>A
NM_000621.4:c.-166T>A NP_000612.1:n.-166T>A
NM_001165947.2:c.160+602T>A NP_001159419.1:n.160+602T>A
NM_000621.5:c.-166T>A MANE Select NP_000612.1:n.-166T>A
NM_001165947.5:c.-78+602T>A NP_001159419.2:n.-78+602T>A
NM_001378924.1:c.-166T>A NP_001365853.1:n.-166T>A
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