Canonical Allele Identifier: CA2089309160

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951066251

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892933G>T , CM000675.2:g.46892933G>T	GRCh38
NC_000013.10:g.47467068G>T , CM000675.1:g.47467068G>T	GRCh37
NC_000013.9:g.46365069G>T	NCBI36
NG_013011.1:g.9102C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413-343C>A MANE Select	ENSP00000437737.1:n.413-343C>A
ENST00000543956.5:c.-77-343C>A	ENSP00000441861.2:n.-77-343C>A
ENST00000378688.8:c.413-343C>A	ENSP00000367959.3:n.413-343C>A
ENST00000542664.3:c.413-343C>A	ENSP00000437737.1:n.413-343C>A
ENST00000543956.4:c.161-343C>A	ENSP00000441861.1:n.161-343C>A
NM_000621.4:c.413-343C>A	NP_000612.1:n.413-343C>A
NM_001165947.2:c.161-343C>A	NP_001159419.1:n.161-343C>A
NM_000621.5:c.413-343C>A MANE Select	NP_000612.1:n.413-343C>A
NM_001165947.5:c.-77-343C>A	NP_001159419.2:n.-77-343C>A
NM_001378924.1:c.413-343C>A	NP_001365853.1:n.413-343C>A