Canonical Allele Identifier: CA2830986216

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46849411A>T , CM000675.2:g.46849411A>T	GRCh38
NC_000013.10:g.47423546A>T , CM000675.1:g.47423546A>T	GRCh37
NC_000013.9:g.46321547A>T	NCBI36
NG_013011.1:g.52624T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-13772T>A MANE Select	ENSP00000437737.1:n.614-13772T>A
ENST00000543956.5:c.125-13772T>A	ENSP00000441861.2:n.125-13772T>A
ENST00000378688.8:c.614-13772T>A	ENSP00000367959.3:n.614-13772T>A
ENST00000542664.3:c.614-13772T>A	ENSP00000437737.1:n.614-13772T>A
ENST00000543956.4:c.362-13772T>A	ENSP00000441861.1:n.362-13772T>A
NM_000621.4:c.614-13772T>A	NP_000612.1:n.614-13772T>A
NM_001165947.2:c.362-13772T>A	NP_001159419.1:n.362-13772T>A
NM_000621.5:c.614-13772T>A MANE Select	NP_000612.1:n.614-13772T>A
NM_001165947.5:c.125-13772T>A	NP_001159419.2:n.125-13772T>A
NM_001378924.1:c.614-13772T>A	NP_001365853.1:n.614-13772T>A