Canonical Allele Identifier: CA955687588
Gene: HTR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46837800A>C , CM000675.2:g.46837800A>C GRCh38
NC_000013.10:g.47411935A>C , CM000675.1:g.47411935A>C GRCh37
NC_000013.9:g.46309936A>C NCBI36
NG_013011.1:g.64235T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-2161T>G MANE Select ENSP00000437737.1:n.614-2161T>G
ENST00000543956.5:c.125-2161T>G ENSP00000441861.2:n.125-2161T>G
ENST00000378688.8:c.614-2161T>G ENSP00000367959.3:n.614-2161T>G
ENST00000542664.3:c.614-2161T>G ENSP00000437737.1:n.614-2161T>G
ENST00000543956.4:c.362-2161T>G ENSP00000441861.1:n.362-2161T>G
NM_000621.4:c.614-2161T>G NP_000612.1:n.614-2161T>G
NM_001165947.2:c.362-2161T>G NP_001159419.1:n.362-2161T>G
NM_000621.5:c.614-2161T>G MANE Select NP_000612.1:n.614-2161T>G
NM_001165947.5:c.125-2161T>G NP_001159419.2:n.125-2161T>G
NM_001378924.1:c.614-2161T>G NP_001365853.1:n.614-2161T>G