Canonical Allele Identifier: CA483555040

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951062473
• MyVariant Identifiers: chr13:g.47466691T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892556T>C , CM000675.2:g.46892556T>C	GRCh38
NC_000013.10:g.47466691T>C , CM000675.1:g.47466691T>C	GRCh37
NC_000013.9:g.46364692T>C	NCBI36
NG_013011.1:g.9479A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.447A>G MANE Select	ENSP00000437737.1:p.Ala149=
ENST00000543956.5:c.-43A>G	ENSP00000441861.2:n.-43A>G
ENST00000378688.8:c.447A>G	ENSP00000367959.3:p.Ala149=
ENST00000542664.3:c.447A>G	ENSP00000437737.1:p.Ala149=
ENST00000543956.4:c.195A>G	ENSP00000441861.1:p.Ala65=
NM_000621.4:c.447A>G	NP_000612.1:p.Ala149=
NM_001165947.2:c.195A>G	NP_001159419.1:p.Ala65=
NM_000621.5:c.447A>G MANE Select	NP_000612.1:p.Ala149=
NM_001165947.5:c.-43A>G	NP_001159419.2:n.-43A>G
NM_001378924.1:c.447A>G	NP_001365853.1:p.Ala149=