Canonical Allele Identifier: CA955688420
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1950825144
gnomAD v3: 13-46867309-T-C
gnomAD v4: 13-46867309-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46867309T>C , CM000675.2:g.46867309T>C GRCh38
NC_000013.10:g.47441444T>C , CM000675.1:g.47441444T>C GRCh37
NC_000013.9:g.46339445T>C NCBI36
NG_013011.1:g.34726A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.613+25081A>G MANE Select ENSP00000437737.1:n.613+25081A>G
ENST00000543956.5:c.124+25081A>G ENSP00000441861.2:n.124+25081A>G
ENST00000378688.8:c.613+25081A>G ENSP00000367959.3:n.613+25081A>G
ENST00000542664.3:c.613+25081A>G ENSP00000437737.1:n.613+25081A>G
ENST00000543956.4:c.361+25081A>G ENSP00000441861.1:n.361+25081A>G
NM_000621.4:c.613+25081A>G NP_000612.1:n.613+25081A>G
NM_001165947.2:c.361+25081A>G NP_001159419.1:n.361+25081A>G
NM_000621.5:c.613+25081A>G MANE Select NP_000612.1:n.613+25081A>G
NM_001165947.5:c.124+25081A>G NP_001159419.2:n.124+25081A>G
NM_001378924.1:c.613+25081A>G NP_001365853.1:n.613+25081A>G
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