Canonical Allele Identifier: CA483739136

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47409062G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834927G>A , CM000675.2:g.46834927G>A	GRCh38
NC_000013.10:g.47409062G>A , CM000675.1:g.47409062G>A	GRCh37
NC_000013.9:g.46307063G>A	NCBI36
NG_013011.1:g.67108C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1326C>T MANE Select	ENSP00000437737.1:p.Asp442=
ENST00000543956.5:c.837C>T	ENSP00000441861.2:p.Asp279=
ENST00000378688.8:c.1326C>T	ENSP00000367959.3:p.Asp442=
ENST00000542664.3:c.1326C>T	ENSP00000437737.1:p.Asp442=
ENST00000543956.4:c.1074C>T	ENSP00000441861.1:p.Asp358=
NM_000621.4:c.1326C>T	NP_000612.1:p.Asp442=
NM_001165947.2:c.1074C>T	NP_001159419.1:p.Asp358=
NM_000621.5:c.1326C>T MANE Select	NP_000612.1:p.Asp442=
NM_001165947.5:c.837C>T	NP_001159419.2:p.Asp279=
NM_001378924.1:c.1326C>T	NP_001365853.1:p.Asp442=