Canonical Allele Identifier: CA609569512
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1466468060

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46837733C>T , CM000675.2:g.46837733C>T GRCh38
NC_000013.10:g.47411868C>T , CM000675.1:g.47411868C>T GRCh37
NC_000013.9:g.46309869C>T NCBI36
NG_013011.1:g.64302G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-2094G>A MANE Select ENSP00000437737.1:n.614-2094G>A
ENST00000543956.5:c.125-2094G>A ENSP00000441861.2:n.125-2094G>A
ENST00000378688.8:c.614-2094G>A ENSP00000367959.3:n.614-2094G>A
ENST00000542664.3:c.614-2094G>A ENSP00000437737.1:n.614-2094G>A
ENST00000543956.4:c.362-2094G>A ENSP00000441861.1:n.362-2094G>A
NM_000621.4:c.614-2094G>A NP_000612.1:n.614-2094G>A
NM_001165947.2:c.362-2094G>A NP_001159419.1:n.362-2094G>A
NM_000621.5:c.614-2094G>A MANE Select NP_000612.1:n.614-2094G>A
NM_001165947.5:c.125-2094G>A NP_001159419.2:n.125-2094G>A
NM_001378924.1:c.614-2094G>A NP_001365853.1:n.614-2094G>A