Canonical Allele Identifier: CA2089311701
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1951100416
gnomAD v4: 13-46895939-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895939A>G , CM000675.2:g.46895939A>G GRCh38
NC_000013.10:g.47470074A>G , CM000675.1:g.47470074A>G GRCh37
NC_000013.9:g.46368075A>G NCBI36
NG_013011.1:g.6096T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-33T>C MANE Select ENSP00000437737.1:n.-33T>C
ENST00000543956.5:c.-78+735T>C ENSP00000441861.2:n.-78+735T>C
ENST00000378688.8:c.-33T>C ENSP00000367959.3:n.-33T>C
ENST00000542664.3:c.-33T>C ENSP00000437737.1:n.-33T>C
ENST00000543956.4:c.160+735T>C ENSP00000441861.1:n.160+735T>C
NM_000621.4:c.-33T>C NP_000612.1:n.-33T>C
NM_001165947.2:c.160+735T>C NP_001159419.1:n.160+735T>C
NM_000621.5:c.-33T>C MANE Select NP_000612.1:n.-33T>C
NM_001165947.5:c.-78+735T>C NP_001159419.2:n.-78+735T>C
NM_001378924.1:c.-33T>C NP_001365853.1:n.-33T>C
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