Canonical Allele Identifier: CA483555006

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466634G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892499G>C , CM000675.2:g.46892499G>C	GRCh38
NC_000013.10:g.47466634G>C , CM000675.1:g.47466634G>C	GRCh37
NC_000013.9:g.46364635G>C	NCBI36
NG_013011.1:g.9536C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.504C>G MANE Select	ENSP00000437737.1:p.Ala168=
ENST00000543956.5:c.15C>G	ENSP00000441861.2:p.Ala5=
ENST00000378688.8:c.504C>G	ENSP00000367959.3:p.Ala168=
ENST00000542664.3:c.504C>G	ENSP00000437737.1:p.Ala168=
ENST00000543956.4:c.252C>G	ENSP00000441861.1:p.Ala84=
NM_000621.4:c.504C>G	NP_000612.1:p.Ala168=
NM_001165947.2:c.252C>G	NP_001159419.1:p.Ala84=
NM_000621.5:c.504C>G MANE Select	NP_000612.1:p.Ala168=
NM_001165947.5:c.15C>G	NP_001159419.2:p.Ala5=
NM_001378924.1:c.504C>G	NP_001365853.1:p.Ala168=