Canonical Allele Identifier: CA2622959735
Gene: HTR2A HGNC NCBI

Linked Data

gnomAD v4: 13-46896105-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46896105A>G , CM000675.2:g.46896105A>G GRCh38
NC_000013.10:g.47470240A>G , CM000675.1:g.47470240A>G GRCh37
NC_000013.9:g.46368241A>G NCBI36
NG_013011.1:g.5930T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.-199T>C MANE Select ENSP00000437737.1:n.-199T>C
ENST00000543956.5:c.-78+569T>C ENSP00000441861.2:n.-78+569T>C
ENST00000542664.3:c.-199T>C ENSP00000437737.1:n.-199T>C
ENST00000543956.4:c.160+569T>C ENSP00000441861.1:n.160+569T>C
NM_000621.4:c.-199T>C NP_000612.1:n.-199T>C
NM_001165947.2:c.160+569T>C NP_001159419.1:n.160+569T>C
NM_000621.5:c.-199T>C MANE Select NP_000612.1:n.-199T>C
NM_001165947.5:c.-78+569T>C NP_001159419.2:n.-78+569T>C
NM_001378924.1:c.-199T>C NP_001365853.1:n.-199T>C
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