Canonical Allele Identifier: CA6977651
Gene: HTR2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2223959
ClinVar RCV Id: RCV004090527
dbSNP Id: rs754348347
ExAC: 13:47466719 C / T
gnomAD v2: 13-47466719-C-T
gnomAD v4: 13-46892584-C-T
MyVariant Identifiers: chr13:g.47466719C>T (hg19) chr13:g.46892584C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46892584C>T , CM000675.2:g.46892584C>T GRCh38
NC_000013.10:g.47466719C>T , CM000675.1:g.47466719C>T GRCh37
NC_000013.9:g.46364720C>T NCBI36
NG_013011.1:g.9451G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.419G>A MANE Select ENSP00000437737.1:p.Arg140Gln
ENST00000543956.5:c.-71G>A ENSP00000441861.2:n.-71G>A
ENST00000378688.8:c.419G>A ENSP00000367959.3:p.Arg140Gln
ENST00000542664.3:c.419G>A ENSP00000437737.1:p.Arg140Gln
ENST00000543956.4:c.167G>A ENSP00000441861.1:p.Arg56Gln
NM_000621.4:c.419G>A NP_000612.1:p.Arg140Gln
NM_001165947.2:c.167G>A NP_001159419.1:p.Arg56Gln
NM_000621.5:c.419G>A MANE Select NP_000612.1:p.Arg140Gln
NM_001165947.5:c.-71G>A NP_001159419.2:n.-71G>A
NM_001378924.1:c.419G>A NP_001365853.1:p.Arg140Gln
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