Canonical Allele Identifier: CA2844288015

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46871933T>G , CM000675.2:g.46871933T>G	GRCh38
NC_000013.10:g.47446068T>G , CM000675.1:g.47446068T>G	GRCh37
NC_000013.9:g.46344069T>G	NCBI36
NG_013011.1:g.30102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+20457A>C MANE Select	ENSP00000437737.1:n.613+20457A>C
ENST00000543956.5:c.124+20457A>C	ENSP00000441861.2:n.124+20457A>C
ENST00000378688.8:c.613+20457A>C	ENSP00000367959.3:n.613+20457A>C
ENST00000542664.3:c.613+20457A>C	ENSP00000437737.1:n.613+20457A>C
ENST00000543956.4:c.361+20457A>C	ENSP00000441861.1:n.361+20457A>C
NM_000621.4:c.613+20457A>C	NP_000612.1:n.613+20457A>C
NM_001165947.2:c.361+20457A>C	NP_001159419.1:n.361+20457A>C
NM_000621.5:c.613+20457A>C MANE Select	NP_000612.1:n.613+20457A>C
NM_001165947.5:c.124+20457A>C	NP_001159419.2:n.124+20457A>C
NM_001378924.1:c.613+20457A>C	NP_001365853.1:n.613+20457A>C