Canonical Allele Identifier: CA2089283313
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1876376411
gnomAD v4: 13-46834779-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46834779C>T , CM000675.2:g.46834779C>T GRCh38
NC_000013.10:g.47408914C>T , CM000675.1:g.47408914C>T GRCh37
NC_000013.9:g.46306915C>T NCBI36
NG_013011.1:g.67256G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.*58G>A MANE Select ENSP00000437737.1:n.*58G>A
ENST00000543956.5:c.*58G>A ENSP00000441861.2:n.*58G>A
ENST00000378688.8:c.*58G>A ENSP00000367959.3:n.*58G>A
ENST00000542664.3:c.*58G>A ENSP00000437737.1:n.*58G>A
ENST00000543956.4:c.*58G>A ENSP00000441861.1:n.*58G>A
NM_000621.4:c.*58G>A NP_000612.1:n.*58G>A
NM_001165947.2:c.*58G>A NP_001159419.1:n.*58G>A
NM_000621.5:c.*58G>A MANE Select NP_000612.1:n.*58G>A
NM_001165947.5:c.*58G>A NP_001159419.2:n.*58G>A
NM_001378924.1:c.*58G>A NP_001365853.1:n.*58G>A
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