Canonical Allele Identifier: CA483739217

Gene: HTR2A

Linked Data

• ClinVar Variation Id: 763882
• ClinVar RCV Id: RCV000942173
• dbSNP Id: rs1593423658
• MyVariant Identifiers: chr13:g.47409128C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834993C>T , CM000675.2:g.46834993C>T	GRCh38
NC_000013.10:g.47409128C>T , CM000675.1:g.47409128C>T	GRCh37
NC_000013.9:g.46307129C>T	NCBI36
NG_013011.1:g.67042G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1260G>A MANE Select	ENSP00000437737.1:p.Lys420=
ENST00000543956.5:c.771G>A	ENSP00000441861.2:p.Lys257=
ENST00000378688.8:c.1260G>A	ENSP00000367959.3:p.Lys420=
ENST00000542664.3:c.1260G>A	ENSP00000437737.1:p.Lys420=
ENST00000543956.4:c.1008G>A	ENSP00000441861.1:p.Lys336=
NM_000621.4:c.1260G>A	NP_000612.1:p.Lys420=
NM_001165947.2:c.1008G>A	NP_001159419.1:p.Lys336=
NM_000621.5:c.1260G>A MANE Select	NP_000612.1:p.Lys420=
NM_001165947.5:c.771G>A	NP_001159419.2:p.Lys257=
NM_001378924.1:c.1260G>A	NP_001365853.1:p.Lys420=