Canonical Allele Identifier: CA2089311735

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951100906

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895976A>C , CM000675.2:g.46895976A>C	GRCh38
NC_000013.10:g.47470111A>C , CM000675.1:g.47470111A>C	GRCh37
NC_000013.9:g.46368112A>C	NCBI36
NG_013011.1:g.6059T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-70T>G MANE Select	ENSP00000437737.1:n.-70T>G
ENST00000543956.5:c.-78+698T>G	ENSP00000441861.2:n.-78+698T>G
ENST00000378688.8:c.-70T>G	ENSP00000367959.3:n.-70T>G
ENST00000542664.3:c.-70T>G	ENSP00000437737.1:n.-70T>G
ENST00000543956.4:c.160+698T>G	ENSP00000441861.1:n.160+698T>G
NM_000621.4:c.-70T>G	NP_000612.1:n.-70T>G
NM_001165947.2:c.160+698T>G	NP_001159419.1:n.160+698T>G
NM_000621.5:c.-70T>G MANE Select	NP_000612.1:n.-70T>G
NM_001165947.5:c.-78+698T>G	NP_001159419.2:n.-78+698T>G
NM_001378924.1:c.-70T>G	NP_001365853.1:n.-70T>G